drjobs Quality Assurance I - Line Ops 1st Shift

Quality Assurance I - Line Ops 1st Shift

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Bloomington - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Simtra BioPharma Solutions (Simtra) is a worldclass Contract Development Manufacturing Organization partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington Indiana US and Halle/Westfalen Germany we offer a wide range of delivery systems including prefilled syringes liquid/lyophilized vials diluents for reconstitution powderfilled vials and sterile crystallization.

Our product types include biologics and small molecules cytotoxics highly potent compounds diluents for reconstitution and vaccines which are all directly injected into patients worldwide. As such there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.

While our primary focus is cGMP manufacturing we offer many support services including formulation and development lyophilization optimization global regulatory support and secondary packaging. Our teams are driven to help clients scale innovate and bring lifechanging medicines to patients worldwide.

Why join Team Simtra Because we:

Make it HAPPEN We bring a growth mindset to every opportunity developing new skillsets and exceeding our expectations and those of our customers.

Make it TOGETHER We work as one respecting each voice and tapping into our unique strengths across teamsso we can solve problems in new ways.

Make it RIGHT We hold ourselves to a high standard of excellencefulfilling our commitments to the customer their patients and our team members.

Make it COUNT We take pride in our daytoday work knowing the impact we make taking on challenges big and small to improve patient health.

The role:

The Quality Associate I Line Operations is a member of the Quality Assurance Line Operations Team reporting directly to the Quality Supervisor. They maintain quality oversight of the manufacturing areas by working closely with manufacturing personnel and performing various checks during manufacturing processes. They also assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Simtra Standard Operating Procedures. This position strives for continuous improvement of processes and contributes to creating an environment where teamwork efficiency safety identity strength purity and quality (SISPQ) are reflected in the finished product.

The responsibilities:

    • Ensures compliance with all worldwide regulatory agency requirements and companyspecific regulations related to quality of product and employee safety.
    • Inprocess review of records to ensure they are complete accurate and follows current Good Manufacturing Practices (cGMP) requirements. Records include batch records and other documents involved in the aseptic processing of drug product.
    • Reports errors deficiencies discrepancies and observations to management. May stop operations when product safety is or may be compromised.
    • Performs Quality functions in classified areas including production oversight manufacturing process assessments and aseptic intervention oversight.
    • Works in collaboration with management teams to prepare for internal and external audits. Assists with timely closure of audit observations and CAPAs.
    • Initiates and authors Nonconformance Reports and corrective and preventative action responses.
    • Conducts biannual inspections of classified areas in preparation for facility shutdown periods.
    • Initiates standard operating procedure (SOP) revisions as needed to support continuous improvement.
    • Ensures that SOPs are current and effective and that staff performs routine tasks according to SOP through direct observation.

Desired qualifications:

    • Bachelors degree (preferred science field) or Associates degree with at least three years of Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience or high school diploma/GED with at least six years Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience
    • Computer proficiency in Microsoft Word Excel and Outlook and the ability to use enterprise software (examples include:JDE BPLM Pilgrim Trackwise etc.

Physical / Safety Requirements

    • Must wear appropriate PPE as required for various manufacturing areas
    • Must be able to gown qualify for Grade A/B areas.
    • Duties will require overtime work including scheduled weekend shifts
    • Position requires standing for long hours but may require sitting for periods of time.

In return youll be eligible for1:

  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • Short and LongTerm Disability Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

1 Current benefit offerings are in effect through 12/31/25

Disclaimer

This job description is intended to provide the minimum knowledge skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.

Equal Employment Opportunity

Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability/handicap status or any other legally protected characteristic.

EEO is the Law
EEO is the law Poster Supplement
Pay Transparency Policy

Data Privacy

To learn more about Simtras approach to data privacy please review the Simtra Recruitment Platform Global Privacy Policy:

Employment Type

Part-Time

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.