Associate Specialist, Quality Product Release-Disposition - Eclaro
Summit, NJ 07901
About the Job
Associate Specialist, Quality Product Release-Disposition
Job Number: 24-00405
Job Number: 24-00405
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for an Associate Specialist, Quality Product Release-Disposition for our client in Summit, NJ.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
- The Associate Specialist is responsible for activities in accordance with corporate policies, standards, procedures, and Global cGMP in support of the QA Disposition Group.
- Functional responsibilities include but are not limited to, ensuring accurate and timely maintenance and review of quality records and manufacturing documentation, inventory management for quality records and manufacturing documentation.
- Additionally, Associate Specialist supports the receipt of executed batch records and the scanning and uploading of documents and may also support document redaction and document printing.
- Employees holding this position will be required to perform any other job-related duties as requested by management.
Responsibilities:
- Proposes solutions for issues and works with management to resolve.
- Follows established procedures and performs work as assigned.
- Understands continuous improvement and improves efficiency and productivity within the group or project.
- Builds relationships internally within and with cross functional teams.
- Supports the receiving of executed batch records.
- Supports the scanning and uploading of quality records.
- Contributes to the goals within the work group.
Required Qualifications:
- Must have knowledge and experience with cGMP manufacturing, quality, and compliance.
- Must possess an independent mindset.
- Work is self-directed.
- Confident in making decisions for non-routine issues.
- Able to prepare written communications and communicate problems to Supervisors with clarity and accuracy.
- Able to effectively multi-task.
- Knowledge of US and global cGMP requirements.
- Excellent verbal and written communication skills.
- B.S. Degree with 1-3 years GMP experience in the pharmaceutical or related industry.
- Equivalent combination of education and experience acceptable.
- Must be skilled in planning and organizing, decision-making, and building relationships.
- Teamwork and ability to work effectively across functional groups and teams to ensure requirements are met.
- Able to effectively multi-task.
If hired, you will enjoy the following Eclaro Benefits:
- 401k Retirement Savings Plan administered by Merrill Lynch
- Commuter Check Pretax Commuter Benefits
- Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
If interested, you may contact:
Chris Imbien
Chris.Imbien@eclaro.com
(843) 872-9257
Chris Imbien | LinkedIn
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
Source : Eclaro