Quality - Associate Specialist - 2nd shift - Monday-Friday - 11a-7:30p - On-Board Companies
Summit, NJ 07901
About the Job
On-Board Scientific is hiring an Quality – Associate Specialist – (2nd shift – 11am-7:30pm – Monday-Friday) of Summit, NJ!
For immediate consideration please send your resume to resumes@onboardusa.com
Subject Line: Position, Title, and State you are located
About Us:Subject Line: Position, Title, and State you are located
On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.
Assistant Scientist based out of Summit, NJ
Position Details:
Position Type: Full Time/ 6-month with a possibility of extension
Job Location: Summit, NJ
Benefits: 401K, Medical, Dental, Vision, and Life Insurance
Compensation: $23.19 per hour.
Shift: 2nd shift – Monday-Friday – 11am-7:30pm
- Must have knowledge and experience with cGMP manufacturing, Quality, and compliance.
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.
Responsibilities:
- Supports the receiving of executed batch records.
- Supports the scanning and uploading of quality records.
- Must be skilled in planning and organizing, decision-making, and building relationships.
- Contributes to the goals within the work group.
- Teamwork and ability to work effectively across functional groups and teams to ensure requirements are met.
- Able to effectively multi-task.
Qualifications:
- Bachelors degree with 1-3 years’ experience in the pharmaceutical or related industry – Equivalent combination of education and experience acceptable.
- 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.
- 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.
- 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.
Apply Today!
www.onboardusa.com
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.
The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”
On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability, or genetics.
24-00332
INDOJ
Source : On-Board Companies