Quality Associate
$52k - $67kBora Pharmaceuticals
About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora's teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer's success more certain. The Quality Associate issues cGMP documentation to operations in support of manufacturing and packaging operations. Reviews executed manufacturing/packaging documentation and dispositions batch release. Performs general quality assurance reviews/approvals. Performs document lifecycle administration functions. ESSENTIAL FUNCTIONS Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category. Compensation and Benefits
We offer a comprehensive benefits package designed to support our employees' wellbeing, including:
Core Values At Bora, our values guide everything we do - from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category.
- Issues cGMP batch records and logbooks to operations in support of manufacturing and packaging operations. Ensures accuracy of documentation issued..
- Perform review of executed manufacturing and packaging batch records to ensure documentation is complete and accurate. Works directly with operations personnel to resolve issues.
- Performs final batch disposition.
- Performs document lifecycle administration functions.
- Ensures compliance and adherence to applicable department procedures. Provides suggestions for enhancements to procedures where necessary.
- Assists Operations in situations requiring investigation. Provides suggestions for documentation resolution.
- Participates in special projects assigned by QA Management.
- High School degree or equivalent and 3 years of experience in an FDA-regulated industry.
- Alternatively, an associate degree in a technical field (e.g., Chemistry, Engineering, etc.) with 1 year of experience or a bachelor's degree in a technical field (e.g., Chemistry, Engineering, etc.) with no experience may be accepted.
- Industry experience must be in a cGMP production environment (preferably Pharmaceutical or Medical Device) with demonstrated proficiency in documentation generation and review.
- Experience in conducting and documenting investigations is a plus.
- Interpersonal, auditing, and proofreading skills required.
- Ability to work independently or with a team; ability to perform detailed work.
- Attention to detail required.
- Competitive salary and performance-based incentives
- Comprehensive health coverage including medical, dental, and vision insurance
- Retirement savings plans with employer matching contributions
- Paid time off
- Professional development opportunities
- Employee wellness programs and resources
- Employee Assistance Program and Mental Health Resources
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category. Compensation and Benefits
We offer a comprehensive benefits package designed to support our employees' wellbeing, including:
- Competitive salary and performance-based incentives
- Comprehensive health coverage including medical, dental, and vision insurance
- Retirement savings plans with employer matching contributions
- Paid time off
- Professional development opportunities
- Employee wellness programs and resources
- Employee Assistance Program and Mental Health Resources
Core Values At Bora, our values guide everything we do - from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category.
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Quality Associate in Maple Grove, MN vacancy
$63.75k - $78.75k
Position Summary The Quality Specialist in our Plymouth, MN location is responsible for assisting in administration of the quality... ..., Skills and Abilities Needed Required: Associates degree and two years of experience in Quality in a regulated industry...SuggestedTemporary workFor contractorsLocal areaMonday to FridayShift work- ...Quality InspectorA Quality Inspector is responsible for ensuring that products meet established standards of quality, safety, and compliance before they move forward in the production process or ship to customers. This role performs detailed inspections using measurement...SuggestedWork at office
$25 - $28.5 per hour
...employees can grow their career and build engineered-to-order products that help power our modern-world technology. Job Summary As a Quality Auditor, you'll ensure that products meet established standards of quality, safety, and compliance by performing detailed...SuggestedTemporary workWork at officeDay shiftAfternoon shift- ...Description Positions in both Champlin & Dayton Job Summary: The Quality Technician ensures that all switchgear and switchboard products... ...Skills and Experience: High school diploma or GED required. Associate degree or technical certification in Electrical Technology, Mechanical...SuggestedWeekly payWork at office
- ...Job Description Job Description Quality Assurance Inspector/Auditor (Reo Plastics, Inc. Maple Grove MN) Compensation: Based on Experience This is a 3rd shift opportunity! ****$1500 Hiring BONUS**** Reo Plastics has an immediate opportunity for a Inspector...SuggestedImmediate startNight shift
$25 - $35 per hour
...production industry, is seeking a dedicated and detail-oriented Quality Technical Administrator to join their team. As a Quality... ...professional development. Upon completion of waiting period associates are eligible for: ~ Medical and Prescription Drug Plans ~...Permanent employmentFull timeTemporary workMonday to FridayFlexible hoursShift work- ...At Nott Company, quality is at the heart of everything we do. We are committed to delivering high-quality products, reliable solutions, and exceptional service to a diverse range of manufacturing and industrial customers. We are currently seeking a Quality Assurance Specialist...Monday to Friday
$25 - $30 per hour
...Quality Assurance Specialist Long-Term Opportunity | Pharmaceuticals | Offers Benefits Job Description As a Quality Assurance Specialist, you will play a crucial role in ensuring the quality of products by auditing facilities and production lines, evaluating raw...Contract workTemporary work$24.76 - $38.87 per hour
...Job Description About the role: As a Quality Control Analyst II, you will execute and review routine in-process, drug substance, and stability test methods in a timely manner. You will use a variety of laboratory instrumentation and computer systems to collect and record...Hourly payMinimum wageFull timeWork at officeLocal areaShift workNight shiftRotating shift- ...job, it’s a chance to engineer smarter solutions, drive industrial innovation and make a lasting impact. In the role of Senior Air Quality Specialist, we'll count on you to: Serve as a technical expert with recognized authority in an area of specialization that...Full timeContract workWork at officeLocal area
$90.5k - $155.2k
...the moments that matter most for our members and employees. Join us in creating a community of connected care, where coordinated, quality service is the norm and every member feels valued. The Quality Analytics Healthcare Analyst is responsible for delivering analytics...Work experience placementWork at office3 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Associate. Be the first to apply!
Related searches
- quality tech Maple Grove, MN
- quality inspection Maple Grove, MN
- quality lead Maple Grove, MN
- air quality Maple Grove, MN
- quality Maple Grove, MN
- water quality Maple Grove, MN
- quality assurance quality control engineer Maple Grove, MN
- quality improvement nurse Maple Grove, MN
- quality manufacturing Maple Grove, MN
- rn quality Maple Grove, MN



