Biopharmaceutical SR. COMMISSIONING & QUALIFICATION LEAD

Job Description

Job Description

Salary : 80,000$ - 110,000$

Previous Pharmaceutical / Biotech experience is mandatory for this role.

MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV. Pharmaceutical expertise includes Oral Solid Dosage, Semi-Solids, Liquid-Dosage (TS and Aseptic), API manufacturing, Biotechnology (Vaccines, Blood Plasma Fractions, Monoclonal Antibodies).

MMR Consulting has offices in Canada, USA, and Australia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers and specialists involved in project management, commissioning and qualification, of equipment, systems and facilities. The work will require working out of the clients facilities.

This role is for Sr. C&Q Lead to work on the commissioning, qualification, startup of upstream and downstream bioprocess systems / equipment in the biopharmaceutical industry, as well as process equipment in pharma / biotech industries. The ideal candidate should possess leadership skills to lead / mentor intermediate / junior specialists. Our client is located in BOULDER , COLORADO, and it will require your presence on-site.

Responsibilities

Provide technical guidance into the commissioning, qualification and start-up of various equipment and facilities.

Lead the development of key qualification deliverables during the project lifecycle to ensure project is well defined, and the action plan to test the system is applicable and relevant.

Lead qualification processes throughout the project lifecycle such as VPP, Risk Assessments, RTM, FCCA / dRA, DQ, FAT, SAT, IQ, OQ and PQ as appropriate to ensure timely completion and to ensure all specifications are met.

Prepare protocols, execute protocols, summarize data, resolve deviations, prepare final reports.

Experience with C&Q parts washer and autoclave is required. Experience with C&Q of other process equipment, utilities, facilities is an asset. Thermal Validation experience is an asset.

• Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
• Engage other departments, as required, for design reviews and decisions.
• Travel may be occasionally required for meetings with clients, equipment fabrication vendors or Factory Acceptance Testing (FATs).
• Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases.
• Client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling / budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals / opportunities), presenting at industry conferences / publishing papers etc.
• Visit construction and installation sites following all site safety requirements.
• Supervise contractors during critical testing of systems and equipment.
• Other duties as assigned by client, and / or MMR, based on workload and project requirements.

Qualifications

Compensation : 80,000$ - 110,000$ based on industry experience.

Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.