Senior Scientist Pharmaceuticals [ ]
Role details
Job location
Tech stack
Job description
We are seeking a skilled and detail-oriented R&D Analytical Method Development Consultant to join our dynamic research and development team. This role is central to ensuring the accuracy, reliability, and compliance of analytical data used throughout the product development lifecycle.
You will be responsible for developing, qualifying, and supporting the pre-validation of analytical methods, performing routine and specialized testing, maintaining laboratory equipment, and contributing to a high-performing, quality-driven R&D environment.
If you are passionate about scientific excellence, have a strong hands-on laboratory background, and thrive in a regulated, collaborative setting, this is an excellent opportunity to grow your career in a mission-driven organization.
Key Responsibilities
Analytical Method Development & Support
Develop, optimize, and support the qualification and pre-validation of analytical methods using techniques such as HPLC, ELISA, UV-Vis spectroscopy, and electrophoresis (e.g., SDS-PAGE).
Assist in troubleshooting method performance issues and implement improvements to enhance robustness and reproducibility.
Contribute to method transfer activities between R&D, QC, and manufacturing teams.
Analytical Testing & Data Integrity
Perform routine and non-routine analytical testing to support development programs, stability studies, and batch release activities.
Follow standard operating procedures (SOPs) and GxP guidelines to ensure accurate, reproducible, and auditable results.
Record, review, and report data in compliance with data integrity standards and internal quality requirements.
Data Analysis & Interpretation
Analyze experimental data using statistical tools such as Minitab to assess method performance and support decision-making.
Interpret results in the context of project objectives under the supervision of scientists or R&D managers.
Support the preparation of technical reports, deviation investigations, and change control documentation.
Laboratory Operations & Maintenance
Conduct regular maintenance, calibration, and troubleshooting of laboratory equipment including HPLC systems, spectrophotometers, and electrophoresis units.
Ensure proper storage, handling, and availability of reagents, standards, and consumables.
Participate in laboratory housekeeping, 5S initiatives, and safety programs to maintain a safe and efficient work environment.
Cross-Functional Collaboration
Work closely with teams in R&D, Quality Control (QC), Quality Assurance (QA), and Manufacturing to support project timelines and deliverables.
Contribute to project meetings, technical discussions, and joint problem-solving efforts.
Training & Continuous Improvement
Support the training of team members on equipment use and laboratory best practices.
Share knowledge and promote adherence to quality, safety, and compliance standards.
Contribute to the development and revision of SOPs, technical documentation, and process improvements., At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:
Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!
Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!
Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.
As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience. We look forward to meeting you!
Requirements
Do you have experience in Minitab?, Do you have a Master's degree?, Bachelor's or Master's degree in Biotechnology, Biochemistry, Pharmaceutical Sciences, Chemistry, or a related field.
Minimum of 3 years of relevant experience in analytical method development, testing, or process support within a pharmaceutical, biotechnology, or life sciences environment.
Proven experience with key analytical techniques: HPLC, ELISA, UV-Vis, and electrophoresis (SDS-PAGE).
Demonstrated ability to maintain and troubleshoot laboratory equipment and ensure calibration compliance.
Strong understanding of GxP principles (GMP, GLP), data integrity, and regulatory compliance.
Proficient in MS Office and data analysis tools such as Minitab.
Excellent organizational, communication, and problem-solving skills.
Fluent in English (written and spoken); proficiency in French and/or Dutch is an advantage.
Ability to work independently and as part of a team in a fast-paced, deadline-driven environment.
Benefits & conditions
Why Join Us?
Be part of a purpose-driven organization at the forefront of scientific innovation.
Work in a collaborative, quality-focused culture that values precision, integrity, and continuous learning.
Access to professional development, training, and career advancement opportunities.
Flexible working arrangements, including hybrid or remote options where applicable.
