QA Specialist (Nights) - Pharmavite
New Albany, OH
About the Job
HELP US BRING THE GIFT OF HEALTH TO LIFE.
Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry. Consumer-driven innovation, high quality products and a promising portfolio, all driven by a team with a shared sense of purpose -- that's Pharmavite. Join us to bring the gift of health to life.
QA Specialist - Days (No Sponsorship)
New Albany, Ohio
Immigration sponsorship is not available for this role.
Position Summary:
Collects, categorizes, and evaluates quality data from manufacturing, reprocessing, packaging processes and the accompanying documents to support Quality and company metrics. Supports Quality Assurance programs and activities, including internal audits, non-conformance investigations, and corrective and preventative action (CAPA) implementation and monitoring. Maintains a critical mindset involving data and process interpretation from material receipt through inspection and post-commercial release. Additional duties include, cross-functional improvement projects and developing timely, accurate, thorough reports for various levels of the organization.
Responsibilities:
Analyze data to identify areas of improvement in the process, especially related to reduction of non-conformances and deviations.
Lead and/or collaborate on non-conformance and CAPA investigations.
Drive root cause identification, analysis, and containment action with urgent, but thorough investigations.
Make clear recommendations for corrective actions based on collaboration and expertise.
Write clear, thorough, and accurate reports and investigations appropriate for internal distribution.
Communicate results, metrics improvements, and necessary escalations to Quality and other department area leaders and/or managers effectively.
Conduct, track and communicate training needs especially in support of Quality and Compliance.
Perform risk-based internal GMP audits and CAPA reports as appropriate.
Provide subject-matter and functional support to internal & external partners.
Work collaboratively to identify and resolve discrepancies in and around manufacturing.
Evaluate existing Quality documentation and procedures for compliance and accuracy.
Update and create documents and procedures as needed to support manufacturing and the quality systems.
Remain aware of and ensures ongoing compliance to internal and industry regulatory requirements.
Able to effectively prioritize work to meet deadlines.
Support department, site, and company KPIs, pQRFT and dQRFT metrics.
Perform other duties as assigned.
Minimum Qualifications:
Education:
4-year college degree in related science field or equivalent industry experience with course work in biology or chemistry and mathematics required.
Certification:
Licenses or certifications are not required but are a plus.
Experience:
A minimum of three years experience in quality or related inspection/investigation activities preferably in a manufacturing environment or an FDA regulated industry.
Knowledge/Skills/Abilities:
Requires:
Ability to problem solve and troubleshoot manufacturing issues related to quality and/or operational issues while meeting deadlines.
Ability to communicate effectively, verbally and writing with multiple levels of employees (employees, leader, manager, etc.) and across multiple functions.
Subject matter expert in their work area to aid in identification of sustainable solutions to address systemic issues.
Working knowledge of equipment, safety, quality and computer systems.
Strong interpersonal, written and oral communications skills.
Statistical and mathematical skills are preferred.
Ability to understand product specifications and how they relate to product manufacturing.
Requirements:
General office environment, ability to sit for long periods of time and pay intense and close attention to detail. Ability to move about an office and a manufacturing facility.
Environment:
Exposure to disagreeable elements is moderate.
Safety:
The incumbent must be able to perform this job safely in accordance with standard operating procedures and good manufacturing practices without endangering the health or safety of self or others.
Supervisory Responsibilities:
None.
OUR OFFER
Here, career paths aren't predefined, and bureaucratic limitations don't exist -- you have the opportunity to grow, learn from industry pioneers, and develop the way you want to. Pharmavite is investing more in the development of our team -- to help us deliver on our purpose and help you achieve your career aspirations. Our environment is geared to fuel curiosity, encourage experimentation, and generate learning as this is the way we develop ourselves and our organization.
Pharmavite is committed to meeting the needs of our employees and their families with a Total Rewards package that's as comprehensive as the vitamins and supplements we deliver to consumers. With competitive compensation programs and standout benefits, we provide employees with optimal health and well-being -- as well as peace of mind. These rewards -- plus our new recognition program -- ensure employees feel supported both at work and home.
Annual Pay
Annual Pay Range
$78,105.00 - $117,158.00This represents the minimum and maximum base salary range for this role, plus annual incentive. Various elements are used to determine a candidate’s starting salary such as job experience, specific skills, and comparison to internal incumbents currently in the role. This information is provided to applicants in accordance with state and local laws.
Visit Pharmavite.com/careers to learn more about our mission and discover an opportunity that's right for you. Health and wellness begins with us.
Pharmavite is an equal employment and affirmative action employer F/M/Disability/Vet/Sexual Orientation/Gender Identity. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to their protected veteran or disabled status, or any protected status. We do not discriminate in employment based on race, color, religion, age, sex, sexual orientation, gender identity, national origin, or any other basis covered by applicable law. All employment is decided based on qualifications, merit, and business need.
Disclaimer
The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications of employees assigned to this job.
CALIFORNIA FAIR CHANCE ACT:
Qualified Applicants with arrest or conviction records will be considered for Employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
JOB ALERT FRAUD:
We have become aware of scams from individuals, organizations, and internet sites claiming to represent Pharmavite in recruitment activities in return for disclosing financial information.
Our hiring process does not include text-based conversations or interviews and never requires payment or fees from job applicants. All of our career opportunities are regularly published and updated on Pharmavite.com’s Careers section.
If you have already provided your personal information, please report it to your local authorities. Any fraudulent activity should be reported to: recruiting@pharmavite.com.
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