This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Standard (Mon-Fri) Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Lead the design and evaluation of formulations and manufacturing processes as well as problem solves for solid, semi-solid, or liquid dosage forms. Engage in the management of clientele, processes, and equipment design for clinical, scale up, and registration batches including tech transfer of projects to and from clients. Manage resources in the Pharmaceutics and Process Technology (PPT) work group to achieve project and team objectives and coach associates in their work group in areas such as the drug development process and Pharmaceutical Development Services (PDS) systems.

Liaise with Project Management, Facility/Equipment Schedulers, Materials Management, Analytical Development and other functional areas to meet project and team objectives. Lead the design/evaluation of formulations and manufacturing processes for solid, semi-solid, or liquid dosage forms.

Lead development of new formulations and scale-up procedures of solid, semi-solid,



or liquid dosage forms at the pre-clinical, clinical, and post marketing stages of drug development.

Manage resources in their PPT work group to achieve project and team objectives. Write protocols for feasibility work and manufacturing batch records and clinical trial materials. Write and ensure timely execution of protocols and provision of results in accordance with current Good Manufacturing Practices and company standards.

Liaise with Project Management, Facility/Equipment Schedulers, Materials Management, Analytical Development and other functional areas to meet project and team objectives.

Coach others in technical matters and systems relating to the PPT.

Promote a safe working setting, report potential hazards and ensure all direct reports follow Environmental Health and Safety procedures.

Work with and advises staff on administrative policies and procedures (if applicable).

Perform alternating or rotating shift work (as required). Bachelor of Science (B.Sc.) in pharmaceutical science or technology.

Previous Project

Management experience.

Previous Supervision and/or leadership experience an asset. Equivalent combinations of education, training, and relevant work experience may be considered.

Good Manufacturing

Practices, Standard Operating Procedures and Food and Drug Administration (FDA) compliance knowledge.

Good organizational, documentation and housekeeping skills.

Ability to work well independently and in a team environment with limited supervision.

Communicates and co-operates with others to meet project and team objectives.

Ability to meet deadlines and prioritize multiple project deliverables.

Demonstrated computer proficiency with Microsoft Office programs.

Proficiency with the English language. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights.

Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.

📌 STAGE - Project Management Officer (Qualité) H/F (Whitby)
🏢 Thermo Fisher Scientific
📍 Whitby