Technical Project Leader I

3 months ago

Whitby, Canada Thermo Fisher Scientific Full time

**Work Schedule**

7 1/2 hr shift

**Environmental Conditions**

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), No eye contacts allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

**Summary**:
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. Handle 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.

**Essential Functions**:

- 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. Lead/participate in problem solving for formulations, equipment and processes.
- Participate in relevant meetings/teleconferences with clients.
- 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.
- Write development reports.
- Develop realistic proposals and timelines.
- 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 environment, report potential hazards and ensure all direct reports follow Environmental Health and Safety procedures.
- Select, develop (goal setting) and evaluate staff to ensure the efficient operation of the function. Work with and advises staff on administrative policies and procedures (if applicable).
- Perform alternating or rotating shift work (as required).

**REQUIRED QUALIFICATIONS**

**Education**:
Bachelor of Science (B.Sc.) in pharmaceutical science or technology.

**Experience**:
Minimum 4 years of previous related experience and general knowledge of drug development.

Previous Project Management experience.

Previous Supervision and/or leadership experience an asset.

**Equivalency**_:_**

Equivalent combinations of education, training, and relevant work experience may be considered.

**Knowledge, Skills and Abilities**:
Strong knowledge and understanding of the drug development process. Demonstrated understanding of equipment, formulations and processes. Good Manufacturing Practices, Standard Operating Procedures and Food and Drug Administration (FDA) compliance knowledge. Demonstrable organizational skills relevant to drug development. Ability to communicate and liaise with clients and other departments. Good organizational, documentation and housekeeping skills. Ability to work well independently and in a team environment with limited supervision. Excellent written and oral communication skills. Communicates and co-operates with others to meet project and team objectives. Ability to meet deadlines and prioritize multiple project deliverables. The ability to motivate and influence. Demonstrated computer proficiency with Microsoft Office programs. Proficiency with the English language.

**Standards and Expectations**:
Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving. Model

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