Senior Associate QC (247 Shift)

Career Category

Job Description

Senior Associate QC Analytics - Overview:

Under minimal supervision responsible for one or more of the following activities in QC including HPLC CE GELs analytical testing characterization method transfer sample and data management and equipment maintenance.

Contributes to team by ensuring the quality of the tasks/services provided by self.
Contributes to the completion of milestones associated with specific projects or activities within team

This role will support manufacturing operations as such work will be as part of a 24/7 shift pattern and flexibility may be necessary.

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Specific Job Duties:
With a high degree of technical flexibility work across diverse areas within the lab.
Plan and perform routine analyses with efficiency and accuracy.
Plan and perform multiple complex routine/ non-routine methods and procedures and a large variety of assays.
Report evaluate back-up/archive trend and approve analytical data.
Troubleshoot solve problems and communicate with stakeholders.
Initiate and/or implement changes in controlled documents.
Participate in audits initiatives and projects that may be departmental or organizational in scope.
Write protocols and perform assay validation and equipment qualification/ verification.
Introduce new techniques to the lab including method transfers reports validations and protocols.
Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
Approve lab results.
May participate in lab investigations.
May provide technical guidance.
May train others.
May contribute to regulatory filings.
May represent the department/organization on various teams.
May interact with outside resources.

Knowledge:
Understanding and application of principles concepts theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
Knowledge of related regulatory/industry considerations compliance issues and/or scientific discovery
Experience in a wide variety of analytical techniques including but not limited to HPLC Capillary Electrophoresis UV and density testing.

Skills:
Take initiative to identify and drive improvements.
Excellent verbal and written communication skills.
a. Strong Technical writing skills for GMP documentation (e.g. investigations procedures change controls)
b. Presentation skills.
c. Escalate issues professionally and on a timely basis.
Decision Making skills.
Teamwork and Coaching others.
Negotiation and Influence skills.
Problem solving skills.
a. Applies research information gathering analytical and interpretation skills to problems of diverse scope
i. Ensures compliance within regulatory environment
ii. Develops solutions to technical problems of moderate complexity
iii. Screens categorizes evaluates reconciles reports and resolves data integrity issues
b. Interprets generally defined practices and methods
c. Able to use statistical analysis tools to perform data trending and evaluation
Project Management and organizational skills including ability to follow assignments through to completion

Compentencies:
Demonstrated ability to work independently and deliver right first-time results
a. Works under minimal direction
b. Work is guided by objectives of the department or assignment
i. Follows procedures
ii. Refers to technical standards principles theories and precedents as needed
iii. May set project timeframes and priorities based on project objectives and ongoing assignments
iv. Recognizes and escalates problems
Demonstrated leadership and communication skills
Auditing documentation and operation process
Demonstrated ability to interact with regulatory agencies

Relevant experience:
Bachelors degree in a science discipline.
5 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
Experience with regulatory compliance in GMP manufacturing and testing of pharmaceutical products.

Salary Range