Job description
Duties and Responsibilities:
This QA Associate III – Analytical position is an individual contributor role and is a member of the QA Team at the Fall River, MA (Unit IV) site. The position reports to the Site QA Lead. The essential and typically expected job duties for this position include but are not limited to the following:
- Review data generated in the laboratory is accordance with stablished criteria set forth in SOPs and established specifications
- Assemble quality data to support management review meeting requirements
- Issuing, reviewing, maintaining, and archiving of laboratory logbooks
- Scanning of laboratory approved finalized qualification for easy accessibility by all department
- Training and execution of internal audits, as required
- Review/approval of calibration records for analytical instrumentation and equipment
- Identify and report any non-conformances and/or discrepancies to management if applicable.
- Complete other duties or participate in project work as assigned by management.
Education and Experience:
- Minimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry, Pharmaceutical Science, or other Life Science discipline.
- Advanced training or education in pharmaceutical quality compliance or related field of study from an accredited college/university.is preferred.
- Minimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP) pharmaceutical work environment.
- Experience in metered dose inhalation (MDI) preferred.
- Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications.
Physical and Work Schedule Requirements:
- Independent, unassisted lifting up to 10 kg, may be required.
- Able to always wear appropriate personal protective equipment (PPE) such as safety glasses, shoe covers, hard hat, lab coat and other PPE, when required.
- Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
- Typical work schedule is Monday through Friday, 9 AM to 5:30 PM. Some weekends may be required based on business needs.
Professional and Behavioral Competencies:
- Must be able to work under general supervision and able to work independently and in a team environment.
- Must be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.
- Must be able to exercise appropriate professional judgment on matters of significance.
- Effective interpersonal relationship skills and the ability to work in a team environment.
- Proficiency in the English language to include usage, spelling, grammar, and punctuation.
- Must have current Good Manufacturing Practices (cGMP) knowledge.
- Must have strong attention-to-detail.
- Must be a self-starter and demonstrate initiative with seeking additional training or direction as needed.
- Must have strong organization and communication skills (written, verbal, and presentation).
- Must be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.
- No employment sponsorship or work visas.
Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit http://www.adeccousa.com/candidate-privacy/. The Company will consider qualified applicants with arrest and conviction records.
About Adecco Life Sciences:
Leveraging the power of relationship building and the Adecco brand, we work to align candidates with permanent positions based on skillset and job requirements. Our personal and tailored approach assures that our candidates are placed into positions that align with their long-term goals. We specialize in recruiting for permanent positions within the Life Sciences industry. Here are just some of the roles we specialize in: - Biotechnology - Pharmaceutical - Clinical Research/Trials - Medical Devices - Quality Assurance - Engineering
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