Description: Conduct standard and advanced laboratory activities with minimal supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, conduct instrument and analytical method troubleshooting; research and recommend corrective actions for out-of-specification and out-of-trend results. Execute approved method transfer protocols, develop and validate analytical methods. Prepare and maintain accurate records in lab notebooks of all testing performed. Analyze data, identify trends and perform basic statistical calculations. Write protocols, reports, methods, standard operation procedures, and submission documents with minimal supervision. Design experimental studies with some supervision. Conduct manufacturing activities for inhalation drug products with minimal supervision. Support the evaluation and introduction of new technologies; be capable of generating new practical ideas; possess good understanding of experimental design. Independently train other scientists. Participate in project activities and support project timelines and proactively contribute to meeting team objectives. Communicate effectively with team members and internal or external customers. Work and communicate effectively with other functional groups. Lead small project tasks effectively, with minimal supervision. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate Health & Safety rules and procedures.Skills:analytical method, troubleshooting, method development, hplc, Development, Biochemistry, Analytic, gmpTop Skills Details:analytical method,troubleshooting,method development,hplcAdditional Skills & Qualifications:Top Skills' Details PhD in Chemistry or Pharmacy or related fields with at least 3 years; MSc with at least 5 years or BSc with at least 8 years of experience in pharmaceutical or related fields. Experience in aerosol sciences preferred. Must possess broad analytical chemistry knowledge in HPLC, GC, UV, FTIR and other related analytical technologies and/or broad knowledge of development and manufacturing of MDI/DPI/Nasal products. Knowledge and understanding of FDA cGMP requirements as they apply to the Pharmaceutical industry. Good understanding of USP methodologies and ICH guidelines. Strong English language skills including writing ability and oral communication.Experience Level:Expert LevelAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Full-time