QC Technical Documentation Lead
QC Technical Documentation Lead
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$ 66500 - 110900
1 Vacancy
Job Description
Use Your Power for Purpose
Every day everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture which is both science and risk-based is flexible innovative and customer-oriented. Whether you are engaged in development maintenance compliance or analysis through research programs your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve. By being part of our team you play a crucial role in maintaining this high standard and making a difference in the lives of patients.
What You Will Achieve
In this role you will:
Conduct and support laboratory operations including sample preparation data collection and analysis
Apply technical skills to assignments ensuring high-quality results and solving moderately complex problems with sound judgment
Follow procedures with general instructions maintaining compliance with regulatory standards and working under moderate supervision
Identify activities to support team goals contributing to overall project success and ensuring adherence to project timelines
Perform testing on clinical and commercial products raw materials and validation samples maintaining a neat and orderly work area
Independently write Standard Operating Procedures technical reports project plans and other documents
Train junior colleagues develop training plans oversee training activities and handle laboratory investigations for events and Out of Stock results
Create review and approve compliant test method transfer and validation protocols reports and equipment qualification/computer validation records
Here Is What You Need (Minimum Requirements)
Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an associates degree with 4 years of experience OR a bachelors degree with 0 years of experience.
- Above years of relevant work experience with the below experience:
- Experience authoring editing reviewing of documents
Bonus Points If You Have (Preferred Requirements)
- Project planning experience
- Lean or Six Sigma experience
- Ability to gain insight into the diverse processes in sterile injectables manufacturing and apply this knowledge in the creation of test methods and procedures.
- Experience and knowledge with SOPs.
- Proven leader either through direct leadership or indirectly through project completion that include multiple team members.
- Proficient in Microsoft Office Applications.
PHYSICAL/MENTAL REQUIREMENTS
- No unique physical requirements
- Mental: Remains organized and positive in ambiguous and fast-paced rapidly changing situations. Ability to analyze data from detailed schedule and risk management tools. Interface effectively with multiple stakeholder groups. Ability to multi-task and be successful working through frequent interruptions of normal routing.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
- Monday-Friday: First Shift
- There are no out of the ordinary travel or shift requirements associated with the position.
- Individual will be expected to work nonstandard schedule as needed to support the business objectives.
Work Location Assignment:On Premise
Last Date To Apply: July 24 2027
The annual base salary for this position ranges from $66500.00 to $110900.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Employment Type
Full-Time
