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QC Technical Manager


Castle Rock, CO 80104
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Job Details

**Closing date: 17th April**

**Job Purpose:**

To lead all Quality Control aspects within the QC laboratory at GC including analytical, regulatory compliance, technical, systems and reporting. The QC laboratory is divided into multiple functional areas, each led by a Technical Manager

**Job Responsibilities:**

+ Manage the QC resources and test activities (direct and non-direct) in order to maintain a high volume laboratory testing function within a diverse QC laboratory operation.

+ Support the laboratory supervisor in their application of local and corporate testing standards as well as EHS standards to ensure a fully compliant, effective and safe QC Operation at GC.

+ Collaborate with Operations, external support / network teams and NPI teams to ensure all testing requirements are delivered within committed lead times and any actions / activities are completed to high standards.

+ Provide technical leadership in support of the site and PGS testing, significant investigations, test registration details and testing of new product introductions to the site.

+ Represent QC function at product, technical and robustness team meetings and lead/drive all associated deliverables.

+ Lead QC product reporting and updates to management and senior management

+ Support the preparation and review of respective QC APQR and process / analytical trend reports.

+ Drive process efficiencies tracking and reporting on improvements including cost, productivity and waste/rework.

+ Lead the QC laboratory function inspection readiness programme ensuring a continuous inspection ready function at all times.

+ Support the development of resource (headcount and equipment) plans for QC Lab function, maintaining an effective capacity planning tool and continuous KPI measurements, and operate within the approved plans.

+ Support management in the continuous enhancement of the QC strategic plan

+ Management of the training, motivation and development of all QC Laboratory function to ensure an agile and flexible workforce, underpinned by a culture of coaching.

+ Accountable for driving a structured and value driven approach to Continuous Improvement with Quality Operations

+ Accountable for management of equipment lifecycle activities within QC

+ Network and liaise as appropriate with other QC professionals inside and external to Pfizer, as necessary, to ensure ongoing knowledge of evolving Quality Laboratory standards.

**Education/Experience** To be successful in this role the following are prerequisites to application:

+ Hold a B.Sc. degree in biological, /chemical sciences, business, or other related technical degree or equivalent experience in regulated industry.

+ Preferable 5 years supervisory experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment.

+ Demonstrated ability to successfully collaborate, influence and lead in a matrix organisation

+ Excellent communication and interpersonal skills

+ Proven record in demonstrating agility

+ Flexibility to travel in support of the role

+ Have experience in representing your functional area on a network team

+ Experience of involvement in technical issue resolution, in a multidisciplinary environment

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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