What are the responsibilities and job description for the MSAT Scientist I - Bioconjugation position at Proclinical Staffing?
MSAT Scientist I - Permanent - Bristol, PA
Drive the science behind next‑generation bioconjugates-where precision meets transformative medicine.
Proclinical is seeking an MSAT Scientist I - Bioconjugation to support the transfer, execution, and ongoing optimization of bioconjugation processes, including ADCs and AOCs, within a cGMP manufacturing environment.
Primary Responsibilities:
The successful candidate will emphasize technical execution, documentation, and hands-on manufacturing support, working collaboratively with cross-functional teams to ensure process accuracy, compliance, and continuous improvement.
Skills & Requirements:
- Degree in Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or related field.
- Basic understanding of cGMP manufacturing environments.
- Exposure to bioconjugation processes such as ADCs or AOCs preferred but not required.
- Familiarity with purification techniques like TFF and chromatography (Protein A, IEX, HIC) is a plus.
- Understanding of aseptic techniques and single-use systems is advantageous.
- Strong attention to detail and documentation practices.
- Ability to follow technical instructions and adapt quickly in a fast-paced environment.
- Basic data analysis skills using Excel or similar tools.
- Effective communication skills and ability to work in cross-functional teams.
- Preferred experience with high-potency APIs, process validation, PPQ, and commercial tech transfer.
- Familiarity with regulatory expectations for complex biologics and bioconjugates is a plus.
Physical Requirements:
- Ability to stand, sit, and walk for extended periods.
- Occasionally lift and move objects up to 30 pounds.
- Perform physical activities such as climbing, stooping, kneeling, and crouching.
- Visual abilities including near and far sight, color vision, and focus.
- Ability to gown into ISO 7-8 suites and adhere to gowning policies.
The MSAT Scientist I's responsibilities will be:
- Adhere to cGMP, GDP, GLP, FDA, and ICH requirements and internal procedures.
- Support technology transfer activities from Process Development or external partners into manufacturing, including document review and execution readiness.
- Assist in authoring and revising batch records, SOPs, BOMs, and other GMP documentation.
- Provide on-the-floor manufacturing support during batch execution, including troubleshooting under supervision.
- Contribute to deviation investigations, root cause analysis, and CAPA implementation with guidance from senior staff.
- Collect, trend, and analyze data to support process performance and continuous improvement.
- Participate in process characterization and scale-up activities.
- Support preparation and execution of PPQ and validation activities as assigned.
- Maintain knowledge of raw materials, consumables, and single-use assemblies used in manufacturing.
- Assist in developing training materials and updating process documentation.
- Collaborate with Manufacturing, Quality, Engineering, and Supply Chain teams.
- Document activities clearly and accurately in accordance with GDP standards.
- Present data and findings to internal teams with guidance from senior MSAT staff.
- Perform other duties as assigned.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy