Job Description Job Description
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.
Position: In Process Inspector II
Location: Bohemia NY 11716
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday to Friday From 11:00 PM to 07:30 AM
Summary: The In Process Inspector role has a significant impact in ensuring the quality and integrity of the production process. Their responsibilities include monitoring and inspecting the various stages of manufacturing to identify any discrepancies while using automatic equipment or visually inspecting labels. Their vigilance and attention to detail play a crucial role in preventing defects, ensuring product safety, and maintaining overall process efficiency.
A Day in the Life:
- Conducting inspections using automatic inspection equipment: Operates and monitors automatic inspection equipment to assess the quality and integrity of pharmaceutical labels during the manufacturing process including setting up the equipment, conducting routine checks, and interpreting the results to identify any defects or change requests from specifications.
- Ensures that labels meet the required standards for accuracy, legibility, and adherence to regulatory requirements.
- Performing QC inspections: Conducts Quality Control (QC) inspections at various stages of the manufacturing process including visually examining labels, verifying label content, conducting accurate counts, checking for proper alignment, and assessing print quality.
- Uses appropriate tools and techniques, to ensure that labels meet the necessary quality standards and complies with regulatory guidelines.
- Documenting and reporting findings: Records all inspection results and documents any non-conformities or deviations identified during the inspections including generating detailed reports, maintaining inspection records, and communicating findings to area supervisor or manager.
- Effective documentation and reporting facilitate traceability, support corrective actions, and contribute to the overall quality assurance process.
Education:
- High school diploma or equivalent required.
Experience:
- Minimum of 1 year of work experience in QA or QC or related field.
- Required: Experience in a cGMP environment.
Knowledge, Skills, Abilities:
- Knowledge of automatic inspection equipment: Possesses a solid understanding of the operation and uses automatic inspection equipment specific to pharmaceutical labeling manufacturing.
- Capable of setting up and calibrating equipment, interprets, and analyses inspection results, and troubleshoots any equipment-related issues.
- Familiarity with automatic inspection equipment and its capabilities is crucial for effective quality control.
- Ability to follow pacing and maintain production flow: Possesses the ability to follow pacing and maintains the production flow including effectively managing their time, ensuring inspections are conducted in a timely manner, and keeping up with the production schedule.
- Maintains attention to detail to prevent any bottlenecks in the manufacturing process.
- Problem tracking and troubleshooting skills: Possesses strong problem tracking and troubleshooting skills and the ability to identify and track issues or deviations during inspections.
- Investigates root causes, and propose appropriate corrective actions.
- Applies analytical thinking and problem-solving abilities to address quality-related problems promptly and effectively.
- Maintains quality standards, minimizes disruptions, and ensures smooth operations in pharmaceutical trial labeling manufacturing.
- Fast-paced environment which relies on teamwork to ensure jobs are completed within established timelines.
TekWissen Group is an equal opportunity employer supporting workforce diversity. TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We're founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen is an equal opportunity employer supporting workplace diversity.
