Validation & Engineering Group, Inc.

QA Specialist II

Validation & Engineering Group, Inc.  •  Carolina, PR (Onsite)  •  6 days ago
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Job Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • QA Specislist II

The Quality Analyst is responsible for resolution of issues with suppliers (investigations and corrective actions), maintenance of supplier status, evaluation and closure of supplier change notifications, supplier scorecards and SQA reports.

Responsibilities:

  • Coordinates resolution of problem relating to quality and performance of purchased materials with suppliers and Manufacturing Quality Assurance.
  • The incumbent monitors and manages implementation of new and existing processes that ultimately impact vendor product quality assurance.
  • Establish and document contact with suppliers concerning quality issues/concerns (i.e. nonconformity, deviation, defect report, waivers, etc.).
  • Perform assessment of supplier change notification (SCN) of incoming material. Monitor supplier change notification review through Plant to ensure a timely completion.
  • Evaluates Specification Acceptance Letter exception and assess need for elevation to area management, as needed.
  • Updates and maintains the System Application Product (SAP) system with current specification date, approval of supplier sites and/or purchasing control.
  • Interfaces with and maintains cooperative relationships with plant departments to assure the total integrity and usability of incoming materials.
  • Serves as an effective liaison and maintains a cooperative relationship with other Quality areas, Plant departments, Bioresearch Center counterparts, and TPMs as needed.
  • Assists section with the follow-up and close out of the management reviews action items upon their implementation.
  • Ensures that all quality goals are met, and all practices and procedures comply with applicable policies and regulations for the Quality areas under his/her responsibility.
  • The Quality Analyst is responsible for resolution of issues with suppliers (investigations and corrective actions), maintenance of supplier status, evaluation and closure of supplier change notifications, supplier scorecards and SQA reports.

Qualifications:

  • Bachelor’s degree in Natural Sciences, Biology, Chemistry or Engineering.
  • Quality related work in the pharmaceutical or medical device Health Care Organization. Total combined minimum years of experience required - 2 years.
  • Key Stakeholders: Suppliers, Purchasing, IQA, Materials Management, TPM's, Technical groups, Manufacturing, Quality Assurance, Compliance, Validation, etc.
    • Good problem solving and analytical skills
    • Good interpersonal relations/communications skills
    • Good verbal and written communication
    • Good negotiation skills
    • Quality related work in the pharmaceutical or medical device Health Care Organization. Total combined minimum years of experience required - 5 years.
  • Technical Skills:
    • Good verbal and written communication.
    • Good problem solving and analytical skills.
    • Good interpersonal relations/communications skills.
    • Good negotiation skills.
    • Good analytical skills.
  • Supplier Management Experience.
  • Must be fully bilingual (English / Spanish).
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Experience in pharmaceutical industry.
  • Preference experience in incoming quality area.
  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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