QuVa Pharma

Manager, Quality Control Lab

QuVa Pharma • $98K — $135K *
Bloomsbury, NJ 08804In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Today
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Job Overview by Ladders

Qualifications

  • BS or MS in chemistry, biology, or related field
  • 5 years experience in a cGMP/FDA regulated environment
  • 3 years in a supervisory or management role
  • Eligibility for drug and background checks
  • Ability to work full-time and authorized in the U.S.

Responsibilities

  • Perform routine testing and release of finished commercial product
  • Maintain accurate and complete records in compliance with SOPs and regulations
  • Implement improvements for analytical methods and instrumentation
  • Report investigations for out-of-spec sterility results
  • Oversee quality in the laboratory operations
  • Manage testing processes from start to finish with minimal supervision
  • Communicate sample scheduling with operations team

Benefits

  • Consistent, full-time work schedule
  • Comprehensive health and wellness benefits
  • 401k with company match
  • Generous paid leave including PLP, PTO, and holidays
  • Opportunities for weekend and overtime work
  • Potential for career advancement in a high-growth company
Full Job Description
Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching and developing staff. Coordinate analytical activities including method transfers and stability testing. Perform release testing for analytical studies.

What the Manager Quality Control -Lab Does Each Day:

  • Test and Release Finished Product routinely for Commercial lots for Potency, Endotoxin, and Sterility
  • Maintain accurate and complete notebook records for all method validation and investigational studies in accordance with SOPs, cGMP, and current GdP
  • Implement improvements to analytical test methods or to instrumentation
  • Write investigation report for OOS for Sterility results
  • Provide quality oversight of Laboratory
  • Responsible for assigned testing and work from beginning to end with minimal supervision
  • Write SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements
  • Communicate with Operation for Scheduling the QC Samples
  • Ensure that analytical methods are validated as efficiently as possible to ensure business milestones are met
  • Provide technical support on an as-needed basis as directed by Director of the Laboratories
  • Manage the budget for the Labs
  • Ensure testing is conducted in a safe manner including but not limited to the proper PPE and ventilation; Any safety issue must be brought to the attention of the Director immediately


Our Most Successful Manager Quality Control- Lab:

  • Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)
  • Is a self-starter and independent learner
  • Promotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization
  • Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform


Minimum Requirements for this Role:

  • BS. or M.S. degree in chemistry, biology or related field required
  • 5 years prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry
  • 3 years of supervisory or management experience required
  • 18+ years of age
  • Able to successfully complete a drug and background check
  • Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas


Any of the Following Will Give You an Edge:

  • Prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry


Benefits of Working at Quva:

  • Set, full-time, consistent work schedule
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 5 paid PLP and 17 PTO days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industry-leading high growth company with future career advancement opportunities
  • The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
  • Range: $98,891 - $135,975 Annually
  • This role is also eligible for an annual incentive bonus, subject to program terms and guidelines


About QuVa Pharma

QuVa Pharma is a pharmaceutical company that specializes in the production and distribution of sterile injectable drugs. The company's products are used in hospitals, clinics, and other healthcare facilities to treat a variety of conditions, including pain, infections, and cancer. QuVa Pharma's facilities are located in Texas and North Carolina, and the company has distribution centers throughout the United States. The company was founded in 2015 and is headquartered in Sugar Land, Texas.
Learn more about QuVa Pharma
Size
500 employees
Industry
Pharmaceuticals & Biotech
Founded
2015
* Ladders Estimates

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