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Tech Ops, Liquid Dose Manufacturing 3rd Shift Support

Pfizer


Location:
Andover, MA
Date:
05/26/2017
Job Code:
1053255-1852
Pfizer
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Job Details

Job Title Tech Ops, Liquid Dose Manufacturing 3rd Shift Support

JobID 1053255-1852

Location: Andover, MA

Description *About Pfizer*

A career at Pfizer offers opportunity, ownership and impact.All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.



*Role Description*

Primarily responsible for the cleaning and sanitization of the Liquid Dose Manufacturing (LDM) suite and the Cell Banking Suite (CBS). This is an entry level position, performing and learning basic techniques, processes and operations. Work is performed in strict compliance with manufacturing standards and all regulatory requirements. Responsible for completing all OJT's and tasks required to perform job duties which include documentation, computers, equipment, work practices within aseptic areas. Demonstrates ability to properly problem solve work-related issues, work with an appropriate level of independence, exercise good judgment/decision making, and effectively work with team members



*Responsibilities*

1. Responsible for sanitization of the Liquid Dose Manufacturing Suite and the Cell Banking Suite. 2. Responsible for maintaining LDM facility equipment in clean, validated working order to be available for the manufacture of drug product according to cGMPs. 3. Responsible for supporting/performing support operations in the manufacture of clinical drug product according to approved batch records. 4. Responsible for supporting the operation of complex pieces of drug product manufacturing equipment. 5. Responsible for generating SCADA reports, maintaining logbooks and other documentation as assigned. 6. Responsible for communicating with peers, supervisors, and interdepartmental groups to provide for an efficient drug production process. 7. Responsible for remaining current on all training requirements and for completing all required procedural and skills training (ILT, OJT, etc.) prior to executing assigned tasks. 8. Responsible for ensuring a safe work environment, and attend training and health/safety courses per job requirements. 9. Responsible for visual inspection of drug product vials10. Responsible for maintaining qualification for use of Personal Air Purifying Respirator



*Qualifications*

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.PHYSICAL/MENTAL REQUIREMENTS1. Must be able to pass sterile gown qualification. 2. Must be able to follow and execute approved standard operating procedures 3. Must be able to pass eye exam for visual inspection activities 4. Job tasks may include frequent bending, lifting of up to 50lbs, and twisting motions. Ability to stand upright for several consecutive hours. Absence of any medical restrictions which could restrict completion of all required duties. Additional demands are area specific. 5. Work must be performed in strict compliance with manufacturing standards and all regulatory requirements.6. Must be able to pass medical clearance for use of Personal Air Purified Respirator.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Normal operations to be performed during third shift (11pm - 7:30am) some overtime work may be required. Most work performed in a Grade A and C controlled environment under cGMP regulations.



*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.





*Tech Ops, Liquid Dose Manufacturing 3rd Shift Support*
*Andover, Massachusetts*
*1053255-1852*


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