BSc Chemistry Jobs at Adare Pharma Solutions | Apply Now
Are you looking for BSc Chemistry Jobs that offer global exposure, career growth, and hands-on pharmaceutical experience? Adare Pharma Solutions is hiring a Formulations Technical Specialist in Vandalia, Ohio, offering an excellent opportunity for chemistry graduates seeking stable and rewarding Chemistry Graduate Jobs in the pharmaceutical manufacturing sector.
About Adare Pharma Solutions
Adare Pharma Solutions is a global leader in pharmaceutical formulation development and manufacturing. Known for its people-first culture, innovation-driven approach, and commitment to quality, Adare offers excellent opportunities for professionals seeking long-term Chemistry Jobs in the pharmaceutical industry. The company supports continuous learning, internal mobility, and career advancement for chemistry graduates and experienced professionals alike.
What can Adare offer you?
- Medical/dental/vision/life – low employee premiums
- 401k with a highly competitive match
- Generous PTO, including floating holidays
- Career growth and internal opportunities
- Tuition reimbursement
- Relocation assistance
- Performance-based bonus
- Employee Recognition Programs
Job Summary
The Formulations Technical Specialist is responsible for supporting projects by developing and maintaining the necessary documentation and tasks required to fulfil project needs. This person will work alongside project teams to drive activities, accelerate timelines, propose ideas for future enhancements/work efficiencies, and provide adequate quality oversight
and expertise for the creation and review of internal quality documents.Responsibilities And Learning Opportunities
- Managing Clinical and Registration Batch Preparation and execution. Responsibilities include:
- Initiate and retain stability samples per SOP procedures
- Scheduling clinical batch execution with R&D, Logistics, and Operations
- Facilitate batch record training with Operations and R&D
- Initiation and completion of System Change Controls.
- Managing actions with multiple departments, reviewing, approving action items until completion, and Change Control closure.
- Serving on the Quality Systems Action Board as the Formulations representative
- Overseeing the qualification of project raw materials by working with Supply Chain and the Global Quality department, with updates on project status and material management from project conception to GMP manufacturing.
- Contribute to the creation and/or review of project DMF and/or other Regulatory documents as needed
- Generating and approving accurate and detailed GMP batch records for clinical trial supplies through Registration manufacturing.
- Generation and revision of SOP, Work Instruction, and Controlled Forms, to support R&D processes
- Managing the procurement of raw materials for both formulation development and GMP batch manufacturing, following the necessary procedures in order to meet aggressive timelines
- Detailed management of formulation projects, processes, and procedures to support Formulation Scientists in meeting aggressive timelines
- Implement procedural changes to existing internal systems to gain efficiencies to get products to clinical trial status earlier by working with Quality Assurance as well as other departments, to implement change
- Participates in the development and implementation of methods, procedures, and regulations necessary for the smooth operation of the business.
- Other miscellaneous tasks as required
Required Skills And Qualifications
- B.S. in Pharmaceutical Sciences, Biochemistry, Chemistry, Chemical Engineering, or a related discipline
- 3+ years of relevant industry working experience.
- Strong understanding of GMPs and associated FDA regulations
- A basic understanding of pharmaceutical formulation development
- A basic understanding of laboratory analytical equipment
