Are you a Senior QA Manager looking to join one of the top Pharmaceutical industries?

Are you looking to further your career and grow?

Do you have experience in Electronic Document Management Systems?

If you answered yes to those three questions, then apply today!

Acara Solutions seeks highly qualified candidates to work on-site with our client in Decatur, IL. Interested?

Here's what you'd do:

• The Senior QA Manager of Document Control and Training will be responsible for the oversight of the documentation and training programs.
• This includes but is not limited to Standard Operating Procedures (SOPs), Specifications, Document Change Requests (DCRs), Master Batch Records (MBRs), Protocols, Training Curriculum, and Quality Management Systems (QMS).
• This individual will work in a detail-oriented, compliant manner to ensure the facility operates in alignment with client policies, procedures, and cGMPs.
• Responsible for the overall direction, coordination, and evaluation of the Document Control and Training departments.
• Lead and assist with maintaining the electronic Document Management System (DMS).
• Lead and assist with maintaining the electronic Learning Management System (LMS) for training.
• Maintain training curricula for positions at the site.
• Responsible for Organizing and archiving cGMP documents on-site.
• Compile and report metrics for Quality Assurance Documentation and Training.
• Evaluate quality processes for alignment with cGMPs and evolving regulatory expectations.
• Assist with investigations and review/approve as needed.
• Review all controlled documents through the Document Change Request (DCR) process.
• Implements and enforces systems, policies, and procedures.
• Assist HR with the creation and delivery of New Hire Orientation (NHO).
• Assist with audits, both internal and external.
• Responsible for performance reviews, goal setting, and personnel development plans for Supervisor, QA Documentation Systems and QA Technicians - Documentation
• Providing regular performance feedback (praise and developmental) to members of the QA Quality Operations team.
• Assists in recruiting, interviewing, and hiring qualified employees to fill open positions.
• Addressing complaints and resolving personnel problems within the department(s).
• Maintaining confidentiality of information.

Here's what you'll get:

Pay: $100000 - $120000/year.

Hours: 40 hours/week.

Length: Direct Placement.

Sounds like a good fit?

APPLY TODAY

About Acara Solutions

Acara is a premier recruiting and workforce solutions provider that helps companies compete for talent. With a legacy of experience in various industries worldwide, we partner with clients, listen to their needs, and customize visionary talent solutions that drive desired business outcomes. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide.

• Bachelor's Degree
• Minimum of 5 years experience in Electronic Document Management System.
• Minimum of 5 years experience in cGMP quality assurance biotechnology, pharmaceutical, or medical device industry.

• Working knowledge, writing, and following of SOPs; document management and control system processes.
• Working knowledge of Microsoft Office Word, Excel, Outlook, and PowerPoint.
• Excellent conceptualizing, analytical, and problem-solving skills.
• Pharmaceutical industry knowledge.
• Effective written and oral communication skills;
• Organizational, and planning skills
• Ability to apply deductive reasoning and analytical thoughts to understand complicated issues
• Demonstrates exceptional time management skills
• Ability to work independently, as well as in a group environment
• Ability to multi-task, set priorities, meet deadlines, and effectively deal with a high level of office stress and
• Ability to maintain confidentiality of work assignments and personnel issues.

Additional Information:

• Upon offer of employment, the individual will be subject to a background check and a drug screen.
• While performing the duties of this job, the employee is regularly needed to sit, stand, walk, talk, and hear.
  The employee needed to use their hands to finger, handle, or feel.
  Specific vision abilities needed by this job include close vision for written work, PC use, and evaluation of test specimens.
• In compliance with federal law, all persons hired will be needed to verify identity and eligibility to work in the United States and to complete the necessary employment eligibility verification form upon hire.