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Quality Assurance Specialist II
PaceĀ® Life Sciences provides a full suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries from our network of CDMO sites, GMP analytical testing laboratories, and manufacturing support service centers.
Our experienced, highly trained industry experts and our investment in state-of-the-art development and manufacturing facilities emphasize our commitment to efficiently advancing client programs through the clinic to commercialization.
We share a common goal to bring real value to people, healthcare professionals, and health businesses worldwide. Driven by our commitment to improving our health, we deliver services that offer hope - and a better, safer, and healthier life for everyone.
This is an onsite, full-time, Monday through Friday from 8 : 00 a.m. to 5 : 00 p.m. position supporting the Woburn, MA location.
Summary :
We are actively seeking a candidate to support our Quality Assurance (QA) systems team in Woburn, MA. The ideal candidate is one who thrives working in a highly dynamic, team-oriented environment, sharing the common goal of providing our clients with the information they need to improve the safety and effectiveness of materials produced and used in pharmaceutical, biologics, and medical device products.
The QA Specialist is directly responsible for overseeing day-to-day QA administration and consulting support. This includes all document control, GLP oversight, data package preparation, administrative tasks, document approvals, report approvals, the performance of internal audits, data auditing, consulting with internal clients to provide guidance and direction, as well as other tasks identified in PLS SOPs.
The Woburn QA Specialist will collaborate with the Salem, NH, QA Director and staff on a routine basis to accomplish harmonization.
Additional tasks include supplier survey approval, client audit hosting, response preparation and QA report authoring, and equipment group support.
The ideal candidate is self-guided and highly motivated, demonstrating a strong sense of initiative, a desire to collaborate with all departments, and an interest in continuing to acquire new knowledge and skills.
Job Responsibilities :
Provide support to all areas of the PLS operation.
Requirements :
Physical / Mental Requirements :
The physical demands described herein represent those that must be met by an employee to successfully perform the job's essential functions.
vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.
Working Environment :
Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gasses, noxious odors, and related items in a lab setting.
OFCCP Statement :
Pace Analytical is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veteran, individuals with disabilities, sexual orientation, or gender identity.
STAR #LI-ONSITE #LI-SM1
This role is onsite, working Monday through Friday, 8 : 00 am to 5 : 00 pm. From time to time, this role will require coming in early, staying late, and occasional weekend work as needed.
Last updated : 2024-03-06
Full Time
$94k-114k (estimate)
02/27/2024
04/11/2024
paceanalytical.in
<25
The job skills required for Quality assurance specialist include Quality Assurance, SOP, Written Communication, Initiative, Calibration, Auditing, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality assurance specialist. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality assurance specialist. Select any job title you are interested in and start to search job requirements.
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