Projektmanager (m/w/d) (Pharmazeut/in)

Scientist (f/m/d)- LC-MS: Drug Product Characterization for Biopharmaceuticals
Permanent employee, Full or part-time · Martinsried (BY)

Purpose of your Job
We are seeking a highly skilled and motivated Scientist specializing in LC-MS (Liquid chromatography-mass spectrometry) to join our analytical team. In this role, you will contribute to the characterization of biopharmaceutical molecules, supporting client projects through advanced analytical techniques. This is an opportunity to work in a dynamic, innovative environment and play a key role in advancing therapeutic development.
Perform LC-MS analyses to characterize biopharmaceutical molecules, ensuring accuracy and compliance with project goals.
Act as a subject matter expert in LC-MS during client projects, providing technical guidance, insights, and solutions tailored to specific needs.
Develop, implement, and validate analytical methods to meet client-specific requirements and regulatory standards.
Collaborate closely with clients and internal teams to ensure seamless execution of projects and alignment with client expectations.
Analyze, interpret, and report complex LC-MS data in a clear and actionable format for clients and project stakeholders.
Optimize and maintain LC-MS equipment, including troubleshooting and calibration.
Stay abreast of advancements in LC-MS technologies and methodologies to drive innovation and improve operational efficiency.
Ensure compliance with quality standards, including documentation and reporting in accordance with regulatory guidelines.

Advanced degree (Ph.D./M.Sc.) in pharmacy, pharmaceutical sciences, (bio)chemistry, chemical engineering, or a related field.
Minimum of 3-5 years of hands-on experience in LC-MS for biopharmaceutical characterization.
Proficiency in operating and maintaining high-resolution mass spectrometers such as Xevo G2-XS QTOF and related software (e.g., UNIFI, Connect, PEAKS Studio, Byos).
Strong analytical skills with a proven ability to handle complex datasets and deliver high-quality reports.
Experience with method development and troubleshooting in a regulated environment (e.g., GMP/GLP).
Effective communication skills in English (German is a plus) with the ability to work collaboratively across teams.
Self-motivated with a proactive approach to problem-solving and innovation.
Let’s formulate innovation together…
Our success & development is created by the people working together @Coriolis. We put People first! That’s why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and customers.

We would like to grow together with you!
Let’s continue building and creating the future now! Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let’s make a difference together!

Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, gender, citizenship or gender identity, color, disability, religion/belief, romantic orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar.

Thank you for your interest! We look forward to receiving your application documents.
Please use our career portal exclusively for this purpose.
We would like to support you from the very beginning to shape your development possibilities here at Coriolis.
For questions or further information, please visit our website or contact us directly.

We are looking forward to your application!

(Technical) Project Manager (f/m/d) - Drug Product Development for Biopharmaceuticals
Permanent employee, Full or part-time · Martinsried (BY)

Purpose of your Job
This role leads drug product development projects focused on formulation development for biopharmaceuticals, ensuring client goals are met with scientific excellence. As the main project leader in the operational team, you’ll oversee technical project planning, resource coordination, and timely delivery. Additionally, you’ll guide team members, fostering high standards in formulation science and project outcomes.
Take over the responsibility to lead and manage drug product development projects with a focus on liquid formulation development of biopharmaceuticals, as antibodies, peptides, oligonucleotides or vaccines for our clients
Take over the lead in the communication with the client from technical end and coordinate internally with other project team members and involved units at Coriolis
Ensure that relevant resources are embedded into the project and that project-related decisions are based on state-of-the-art scientific principles
Perform experimental project planning, coordination, resource management, and execution (supported by project team members)
Ensure timely delivery of project milestones within budget, scope and desired quality
Ensure that project deliverables, i.e. experimental plans, experimental data, data presentations and reports are prepared timely and according to the required quality standards
Take over the responsibility for interpretation of scientific data and the drawing of final conclusions; compile and present scientific data presentations as well as technical reports
Act in the role as a drug product development expert (individually with a different focus based on your experience) and provide support to team members

University degree in pharmacy, (bio)chemistry, biology, or related field, PhD beneficial
A minimum of 4-5 years of relevant working experience
Proven ability in leading drug product development programs
Profound expertise / scientific knowledge in liquid formulation development and analytical characterization of biopharmaceuticals
Team player with strong motivation and inter-personal skills
Open for new ideas and tasks, can-do attitude and hands on mentality
Excellent verbal and written communication skills in English and German
Let’s formulate innovation together…
Our success & development is created by the people working together @Coriolis.
We put People first! That’s why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and clients.

We would like to grow together with you!
Let’s continue building and creating the future now, join our team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience.
We offer an attractive work space at the Martinsried site. Let’s make a difference together!

Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, gender, citizenship or gender identity, color, disability, religion/belief, romantic orientation, marital status, age or individual preferencies. Different backgrounds, experiences and ideas push us further and raise the bar.

Thank you for your interest! We look forward to receiving your application documents.
Please usethe application-button exclusively for this purpose.
We would like to support you from the very beginning to shape your development possibilities here at Coriolis.
For questions or further information, please visit our website or contact us directly.

We are looking forward to your application!

GMP Project Manager - Analytical Science (f/m/d)
Permanent employee, Full or part-time · Martinsried (BY)

Purpose of your Job
At Coriolis Pharma, we are committed to ensuring the successful production and commercialization of our clients' biopharmaceutical products. As a GMP Project Manager, you will leverage your scientific expertise and project leadership skills to manage complex customer projects in the GMP-regulated environment. You will oversee both the execution of laboratory operations and the strategic management of client projects, ensuring that scientific objectives are met within quality and regulatory frameworks. As a GMP Project Manager, you will manage the execution of customer projects, coordinate laboratory activities, and ensure compliance with project requirements. Your responsibilities will include:

Project Management: Oversee and manage client projects and project teams, ensuring that all project milestones, timelines, and budgets are met. Coordinate with cross-functional teams to ensure efficient and timely project execution.
Client Relationship Management: Foster strong client relationships by ensuring clear communication, setting expectations, and addressing concerns to ensure client satisfaction and the success of their projects.
Support development: Supervise, instruct and support on-boarding of new team members. Ensure efficient knowledge transfer within project teams.
Scientific Oversight: Oversee and actively contribute to the execution of experiments following SOPs, pharmacopoeias, and project-specific requirements. Lead the analytical strategy, utilizing laboratory techniques.
Data Analysis & Reporting: Analyze experimental data, interpret results, and prepare comprehensive reports for both internal teams and clients. Collaborate closely with project stakeholders to assess progress and adapt strategies as necessary.Equipment & Compliance Management: Oversee the qualification, maintenance, and proper functioning of analytical equipment, ensuring compliance with GMP standards. Manage equipment calibration, validation, and maintenance activities, ensuring that all systems meet regulatory requirements.
Quality Assurance & Regulatory Compliance: Lead efforts to ensure full adherence to QA and QC processes. Manage deviations, CAPAs, change controls, and out-of-specification (OOS) results, ensuring that all actions align with regulatory guidelines.
Cross-Functional Collaboration: Drive and contribute to cross-functional teams, managing resources, ensuring smooth project execution, and identifying opportunities for improvement. Assist in the preparation of validation protocols, reports, and testing procedures.

A degree in pharmacy, (bio)chemistry, biotechnology, biophysics, or a related field (PhD preferred).
Proven experience in managing large-scale projects and leading of project teams
Ability to simplify and reduce complex tasks into the key elements.
Flexibility in working in different environments (GMP and R&D) as well as willingness to work across time zones
In-depth understanding of GMP regulations, quality management systems, and regulatory standards.
Practical experience in a GMP-regulated laboratory environment, with expertise in laboratory techniques such as HPLC, UV-Vis spectroscopy, and particle size analysis is preferred.
Strong background in analytical method development, validation, and qualification.
Strong communication skills in English, both written and verbal, and the ability to collaborate effectively with cross-functional teams and clients.
Let’s formulate innovation together…
Our success & development is created by the people working together @Coriolis.
We put People first! That’s why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and clients.

We would like to grow together with you!
Let’s continue building and creating the future now, join our team of cur...

Quality Manager (gn) Laboratories
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.

Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines.

To support our team in Martinsried near Munich, we are seeking a highly motivated and detail-oriented Quality Manager for this full-time and permanent position, to begin work as soon as possible. As a Quality Manager, you will play a crucial role in ensuring compliance with our Quality Management System (QMS) and maintaining high standards of quality across our organization.

The main tasks of this role include the following:

Conduct quality checks on documents created by various departments
Review analytical summary documents and reports for accuracy and compliance
Provide input and review method qualification/validation processes
Handle internal changes, deviations, Corrective and Preventive Actions (CAPA), trend analysis, and risk assessments
Support internal training programs and self-inspections
Write and review Standard Operating Procedures (SOPs) and contribute to the continuous improvement of the QMS
Serve as a backup for the training process

The general responsibilities of this position are:

Ensure compliance with QMS requirements
Take accountability for deadlines within your area of expertise
Continuously improve internal quality standards and workflows
Independently plan and prepare department-related documents and activities, coordinating with other departments
Participate in technical team meetings (both internal and external) as a specialist
Provide technical guidance to colleagues
Prepare quality management (QM) documents
Participate in internal and external audits and inspections
Establish and coordinate complex interactions and relationships with internal departments

Bachelor’s or Master’s degree in a relevant field
Minimum of 3 years of experience in pharmaceutical Quality Assurance (QA) and compliance functions, ideally with a focus on analytical laboratories
Fluent in both English and German
Excellent problem-solving skills
Good organizational abilities
Results-oriented mindset
Ability to work independently
Effective presentation and communication skills
Comfortable working under pressure

Flexible working time
Hybrid work
30 days paid vacation
Formycon pension
Group accident insurance
Formycon card
Continuing education offers
Team spirit, great working atmosphere and much more!

Bring us your skills and energy, and shape your own career in a stimulating and open work environment. We are looking for highly motivated individuals who are ready to take on new challenges with enthusiasm and personal commitment. Working at Formycon means being part of a smart, innovative team with minimal hierarchy and opportunity to share your own ideas.

Quality Manager (gn) Laboratories
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.

Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines.

To support our team in Martinsried near Munich, we are seeking a highly motivated and detail-oriented Quality Manager for this full-time and permanent position, to begin work as soon as possible. As a Quality Manager, you will play a crucial role in ensuring compliance with our Quality Management System (QMS) and maintaining high standards of quality across our organization.

The main tasks of this role include the following:

Conduct quality checks on documents created by various departments
Review analytical summary documents and reports for accuracy and compliance
Provide input and review method qualification/validation processes
Handle internal changes, deviations, Corrective and Preventive Actions (CAPA), trend analysis, and risk assessments
Support internal training programs and self-inspections
Write and review Standard Operating Procedures (SOPs) and contribute to the continuous improvement of the QMS
Serve as a backup for the training process

The general responsibilities of this position are:

Ensure compliance with QMS requirements
Take accountability for deadlines within your area of expertise
Continuously improve internal quality standards and workflows
Independently plan and prepare department-related documents and activities, coordinating with other departments
Participate in technical team meetings (both internal and external) as a specialist
Provide technical guidance to colleagues
Prepare quality management (QM) documents
Participate in internal and external audits and inspections
Establish and coordinate complex interactions and relationships with internal departments

Bachelor’s or Master’s degree in a relevant field
Minimum of 3 years of experience in pharmaceutical Quality Assurance (QA) and compliance functions, ideally with a focus on analytical laboratories
Fluent in both English and German
Excellent problem-solving skills
Good organizational abilities
Results-oriented mindset
Ability to work independently
Effective presentation and communication skills
Comfortable working under pressure

Flexible working time
Hybrid work
30 days paid vacation
Formycon pension
Group accident insurance
Formycon card
Continuing education offers
Team spirit, great working atmosphere and much more!

Bring us your skills and energy, and shape your own career in a stimulating and open work environment. We are looking for highly motivated individuals who are ready to take on new challenges with enthusiasm and personal commitment. Working at Formycon means being part of a smart, innovative team with minimal hierarchy and opportunity to share your own ideas.

Quality Manager (gn) Laboratories
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.

Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines.

To support our team in Martinsried near Munich, we are seeking a highly motivated and detail-oriented Quality Manager for this full-time and permanent position, to begin work as soon as possible. As a Quality Manager, you will play a crucial role in ensuring compliance with our Quality Management System (QMS) and maintaining high standards of quality across our organization.

The main tasks of this role include the following:

Conduct quality checks on documents created by various departments
Review analytical summary documents and reports for accuracy and compliance
Provide input and review method qualification/validation processes
Handle internal changes, deviations, Corrective and Preventive Actions (CAPA), trend analysis, and risk assessments
Support internal training programs and self-inspections
Write and review Standard Operating Procedures (SOPs) and contribute to the continuous improvement of the QMS
Serve as a backup for the training process

The general responsibilities of this position are:

Ensure compliance with QMS requirements
Take accountability for deadlines within your area of expertise
Continuously improve internal quality standards and workflows
Independently plan and prepare department-related documents and activities, coordinating with other departments
Participate in technical team meetings (both internal and external) as a specialist
Provide technical guidance to colleagues
Prepare quality management (QM) documents
Participate in internal and external audits and inspections
Establish and coordinate complex interactions and relationships with internal departments

Bachelor’s or Master’s degree in a relevant field
Minimum of 3 years of experience in pharmaceutical Quality Assurance (QA) and compliance functions, ideally with a focus on analytical laboratories
Fluent in both English and German
Excellent problem-solving skills
Good organizational abilities
Results-oriented mindset
Ability to work independently
Effective presentation and communication skills
Comfortable working under pressure

Flexible working time
Hybrid work
30 days paid vacation
Formycon pension
Group accident insurance
Formycon card
Continuing education offers
Team spirit, great working atmosphere and much more!

Bring us your skills and energy, and shape your own career in a stimulating and open work environment. We are looking for highly motivated individuals who are ready to take on new challenges with enthusiasm and personal commitment. Working at Formycon means being part of a smart, innovative team with minimal hierarchy and opportunity to share your own ideas.

Quality Manager (gn) Laboratories
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.

Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines.

To support our team in Martinsried near Munich, we are seeking a highly motivated and detail-oriented Quality Manager for this full-time and permanent position, to begin work as soon as possible. As a Quality Manager, you will play a crucial role in ensuring compliance with our Quality Management System (QMS) and maintaining high standards of quality across our organization.

The main tasks of this role include the following:

Conduct quality checks on documents created by various departments
Review analytical summary documents and reports for accuracy and compliance
Provide input and review method qualification/validation processes
Handle internal changes, deviations, Corrective and Preventive Actions (CAPA), trend analysis, and risk assessments
Support internal training programs and self-inspections
Write and review Standard Operating Procedures (SOPs) and contribute to the continuous improvement of the QMS
Serve as a backup for the training process

The general responsibilities of this position are:

Ensure compliance with QMS requirements
Take accountability for deadlines within your area of expertise
Continuously improve internal quality standards and workflows
Independently plan and prepare department-related documents and activities, coordinating with other departments
Participate in technical team meetings (both internal and external) as a specialist
Provide technical guidance to colleagues
Prepare quality management (QM) documents
Participate in internal and external audits and inspections
Establish and coordinate complex interactions and relationships with internal departments

Bachelor’s or Master’s degree in a relevant field
Minimum of 3 years of experience in pharmaceutical Quality Assurance (QA) and compliance functions, ideally with a focus on analytical laboratories
Fluent in both English and German
Excellent problem-solving skills
Good organizational abilities
Results-oriented mindset
Ability to work independently
Effective presentation and communication skills
Comfortable working under pressure

Flexible working time
Hybrid work
30 days paid vacation
Formycon pension
Group accident insurance
Formycon card
Continuing education offers
Team spirit, great working atmosphere and much more!

Bring us your skills and energy, and shape your own career in a stimulating and open work environment. We are looking for highly motivated individuals who are ready to take on new challenges with enthusiasm and personal commitment. Working at Formycon means being part of a smart, innovative team with minimal hierarchy and opportunity to share your own ideas.

Quality Manager (gn) Laboratories
Formycon is an international leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. With an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.

Our focus is on treatments in ophthalmology and immunology as well as for other key chronic diseases. Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines.

To support our team in Martinsried near Munich, we are seeking a highly motivated and detail-oriented Quality Manager for this full-time and permanent position, to begin work as soon as possible. As a Quality Manager, you will play a crucial role in ensuring compliance with our Quality Management System (QMS) and maintaining high standards of quality across our organization.

The main tasks of this role include the following:

Conduct quality checks on documents created by various departments
Review analytical summary documents and reports for accuracy and compliance
Provide input and review method qualification/validation processes
Handle internal changes, deviations, Corrective and Preventive Actions (CAPA), trend analysis, and risk assessments
Support internal training programs and self-inspections
Write and review Standard Operating Procedures (SOPs) and contribute to the continuous improvement of the QMS
Serve as a backup for the training process

The general responsibilities of this position are:

Ensure compliance with QMS requirements
Take accountability for deadlines within your area of expertise
Continuously improve internal quality standards and workflows
Independently plan and prepare department-related documents and activities, coordinating with other departments
Participate in technical team meetings (both internal and external) as a specialist
Provide technical guidance to colleagues
Prepare quality management (QM) documents
Participate in internal and external audits and inspections
Establish and coordinate complex interactions and relationships with internal departments

Bachelor’s or Master’s degree in a relevant field
Minimum of 3 years of experience in pharmaceutical Quality Assurance (QA) and compliance functions, ideally with a focus on analytical laboratories
Fluent in both English and German
Excellent problem-solving skills
Good organizational abilities
Results-oriented mindset
Ability to work independently
Effective presentation and communication skills
Comfortable working under pressure

Flexible working time
Hybrid work
30 days paid vacation
Formycon pension
Group accident insurance
Formycon card
Continuing education offers
Team spirit, great working atmosphere and much more!

Bring us your skills and energy, and shape your own career in a stimulating and open work environment. We are looking for highly motivated individuals who are ready to take on new challenges with enthusiasm and personal commitment. Working at Formycon means being part of a smart, innovative team with minimal hierarchy and opportunity to share your own ideas.