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Stability Scientist

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Company :
Bristol-Myers Squibb

Location :
Devens, Massachusetts

Expiry Date :
Wed, 16 Dec 2020 23:59:59 GMT

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Description :
Job Details Full-timeEstimated: $87,000 – $110,000 a year4 hours ago Benefits – Health insurance Qualifications – FDA regulations – Technical writing – CGMP – Microbiology – Continuous improvement – Bachelor’s degree – Doctoral degree Full Job Description At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Stability Scientist is responsible for activities related to the global stability studies. Activities include protocol authoring, LIMS study approval, stability data evaluation and trending, authoring stability reports and stability sections of CMC regulatory filings. The stability scientist supports the Global Biologics Stability program for BMS and Third Party Manufacturers (TPM). The stability Scientist will also assist with Stability Assessments, Study Generation and Sample Management. Activities are performed in accordance with cGMP and Company SOPs and as requested by management. MAJOR DUTIES AND RESPONSIBILITIES: – Execute stability program activities for the commercial biologic products. Author master stability protocols, stability study protocols. Evaluate stability study LIMS build for accuracy. Critically review stability documents for consistency and quality. – Work in collaboration with Global Regulatory Sciences, CMC teams and technical experts to author CMC stability sections of initial and post approval HA submissions. – Author site APQR/APR and end to-end APQR/APR and present the data at internal meetings. – Author ad-hoc stability filings and submissions. Respond to HA stability questions. Complete and close all stability studies. – Point person for global rollout of observations that may impact stability programs and develop strategies to close gaps/mitigation. – Approve, identify, write and revise SOPs. Assist with development of company directives – Data entry and verification in the electronic laboratory information management system (LIMS) – Support Health Authority inspections and internal inspections – Act, escalate, identify information regarding stability program that may impact lab capacity, product studies or regulatory commitments directly and promptly to management – Works according to cGMP requirements and HA expectations. Qualifications – External KNOWLEDGE AND SKILL – Minimum of – 2 years (PhD)/ 6-8 years (MS)/ 8-10 years (BS) relevant cGMP experience in biopharma at BMS or other company – Knowledge and understanding of ICH Guidelines (Q1A, Q5C), US/EU/ROW stability requirements, and industry best practices. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a biologics manufacturing facility. – Excellent technical writing skills. Experience authoring CMC filing sections – Ability to work collaboratively in a team matrix environment – Experience with evaluating and interpreting stability data using statistics and statistics software – Applied knowledge and good understanding of analytical and/ or Microbiology techniques – Exhibit strong leadership and decision making skills. Develop strategies for solving complex problems/issues; recommending and driving implementation of solutions. – Experience in Operational Excellence, with proven record of accomplishment in continuous improvement. – Prior experience with stability programs and demonstrated expertise in Biologics or Protein Therapeutic molecules – Works independently with a demonstrated ability to recognize anomalous trends or results. Able to prioritize objectives from multiple projects, and deliver according to overall strategy. – Use computer software/programs: Microsoft Office applications, SAP, LIMS, Trackwise, JMP, etc. – Front room FDA/Inspectional experience is preferred. DECISION MAKING – Scientist works on problems of diverse scope in which analysis of situation or data requires evaluation of identifiable factors. – Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. – Acts as an advisor to subordinate staff to resolve problems. Develops performance requirements and evaluates subordinates accordingly. Establishes and recommends changes to policies which affect subordinate organization. – Erroneous decisions or failure to achieve goals results in itional costs and personnel, and serious delays in overall schedules. SUPERVISION RECEIVED – Scientist receives assignments in the form of objectives and establishes goals to meet objectives. Work is reviewed and measured based on meeting established objectives and schedules. Identifies and reports any discrepancies from normal practices or procedures to senior management, recommending and implementing corrective actions. SUPERVISION EXERCISED – Direct Supervision of Exempt/ non-exempt employees may be required BMSBL Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to our individual talents and diverse perspectives in an inclusive culture, our d values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Show full job description Apply Now