You haven't searched anything yet.
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 of all 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. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; 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
Full Time
$88k-107k (estimate)
06/14/2023
05/05/2024
paceanalytical.in
<25
The job skills required for Quality Assurance Specialist II include Quality Assurance, SOP, Initiative, Written Communication, Internal Audit, Attention to Detail, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Assurance Specialist II. 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 II. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Quality Assurance Specialist II positions, which can be used as a reference in future career path planning. As a Quality Assurance Specialist II, it can be promoted into senior positions as a Quality Assurance Specialist III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Assurance Specialist II. You can explore the career advancement for a Quality Assurance Specialist II below and select your interested title to get hiring information.