Formulation Scientist I
Primary Talent Partners · Rahway, NJ · 1 mo ago
On-siteAnalyst$24–$34/hrContract
About the role
Primary Talent Partners has a 12 month contract opening for a Formulation Scientist I to join a multinational pharmaceutical company for an onsite position operating out of Rahway, NJ. The position is a W-2 contract (12 months, extensions likely, conversion possible). The employer cannot support C2C or provide visa sponsorship; no benefits or PTO are offered, but an ACA‑compliant medical package is available for enrollment.
Responsibilities
- Design and execute hypothesis‑driven formulation and process‑development experiments for sterile pharmaceutical products.
- Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable.
- Support processing activities for solution or lyophilized formulations, or other dosage‑form preparation techniques as required.
- Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle‑size measurements, dynamic light scattering, and HPLC.
- Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports.
- Draft, review, and execute protocols supporting laboratory batches and process‑development activities.
- Maintain clear, accurate, and contemporaneous laboratory records.
- Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment.
- Collaborate with cross‑functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables.
- Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes.
- Perform all work safely and in compliance with applicable site procedures and safety policies.
Qualifications
- B.S. or M.S. degree, or equivalent, in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field is required.
- Bachelor’s with 2‑3 years or master’s with 1‑2 years of experience.
Skills
Required
- Excellent hands‑on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field.
- Strong written and verbal communication skills.
- Self‑driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn.
- Ability to work effectively as part of a team and interface with cross‑functional scientific professionals.
Desired
- Experience with biologics and sterile formulation.
- Pharmaceutical industry experience in formulation and/or process development.
- Understanding of formulation and aseptic processes in a non‑GMP/GLP environment.
- Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization.
- Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS‑PAGE, or UV/Vis.
- Ability to manage multiple priorities in a fast‑paced environment and adapt to changing project needs.
- Statistical software such as JMP.
Key Skills
- Strong hands‑on wet‑lab experience
- Biologics formulation development
- Preparation of formulation buffers, reagents, and protein formulations
- Execution of development batches
- Aseptic filling of vials and prefilled syringes
- Setup and management of stability studies
- Good laboratory practices
- Sample submission and cross‑functional collaboration
- Data analysis, interpretation, graphing, and plotting
- Proficiency in Microsoft Excel
- Experience with osmolality, pH, and viscosity testing
Benefits
No benefits or PTO are provided; however, an ACA‑compliant medical package is available for enrollment.
Pay
$24.00/hr – $34.00/hr based on experience and academia.