Job Overview
Primary technical contact for client communication.
Execute projects to support formulation development, tech transfer, scientific data analysis, registration batches or clinical trials manufacture.
Maintain systems and facilities in a cGMP status and manufacture supplies in a compliant manner.
Generate data and reports to support product development, validation or registration in a compliant manner.
Secondary SME for regulatory and customer audits as well as technical meetings on clinical trials, formulation or tech transfer manufacturing at Morpeth.
Key Responsibilities
1. Primary product development person for Piramal projects.
2. Co-ordinate with Project management in the execution of development projects.
3. Co-ordinate with Production groups for the introduction of new products.
4. Maintain the department facilities, records, equipment and procedures in line with GMP.
5. Develop skills and knowledge relevant to the operations.
6. Maintain the departmental compliance to GMP and procedures for operation of rooms and equipment, record keeping and reports.
7. Conduct experiments which increase the company understanding of products it manufactures or intends to manufacture.
8. Ensure that R&D activities comply with QMS and EHS requirements. Manage and protect R&D assets as intellectual property. Budget and manage expenses.
9. Develop strong, collaborative relationships with other departments/groups and foster an environment of knowledge sharing and cross-functional teamwork.
10. Keep up to date with current trends and advances in Pharmaceutical sciences for oral dosage forms.
Equal Employment Opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.
We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms.
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