This is an exceptional opportunity to join a global biopharmaceutical leader in North Chicago, IL, focusing on advancing critical drug product development. You will be instrumental in the process development of parenteral drug products, with a specific focus on cutting-edge therapeutics like antibody-drug conjugates (ADCs). The site for this role is a dynamic, state-of-the-art facility dedicated to innovation and patient health. This hybrid position offers a chance to apply your expertise in formulation, stability evaluation, and process optimization to bring life-changing treatments from clinic to commercialization.
location: North Chicago, Illinois
job type: Contract
salary: $50.00 - 57.48 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Independently design and execute lab studies to develop robust manufacturing processes for clinical and commercial products.
- Support the process development of parenteral drug products, focusing on Antibody Drug Conjugates (ADCs).
- Design and execute studies evaluating the chemical and physical stability of biologics under various stress conditions.
- Generate, analyze, and interpret precise, reliable, and reproducible data in a timely manner.
- Contribute to and draft scientific reports and CMC documentation.
- Develop robust dosage forms by evaluating physical stresses from manufacturing conditions (e.g., freeze thaw, lyophilization, filtration).
qualifications:
Required Skills & Experience:
- Education: Bachelor's Degree with typically 7+ years of experience, OR Master's degree with 3+ years of experience, OR PhD with 0+ years of experience in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar scientific area.
- Direct experience supporting the process development of parenteral drug products.
- Experience with antibody drug conjugates (ADCs) or similar complex biologics.
- Ability to design and execute studies evaluating the stability (chemical & physical) of biologics.
- Proven ability to interpret results, draw scientific conclusions, and suggest/pursue relevant follow-up experiments.
- Demonstrated scientific writing skills and strong verbal communication skills.
- Experience with commercial site scale-up and tech transfer.
- Experience with physical stresses arising from manufacturing process conditions (e.g., freeze thaw, mixing, filtration, filling, and lyophilization).
skills: Chemistry, Chemistry Manufacturing and Controls (CMC)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
