Biovation Labs LLC
Benefits Offered:
Medical
Dental
Vision
401K with company match
PTO
11 Paid Holidays
4/10 schedule Monday - Thursday (Maybe asked to work overtime, weekends, or Holidays depending on business needs)
PM Shift 4 PM - 2:30 AM
Job Summary:
The Quality Technician II plays a key role in ensuring product integrity and regulatory compliance throughout the manufacturing process. This position is responsible for performing in-depth inspections, testing, and documentation of raw materials, in-process components, and finished goods. The role supports quality initiatives by enforcing GMP standards, executing internal audits, resolving non-conformances, and implementing corrective actions. Acting as a mentor and indirect lead to junior quality staff, the Quality Technician II collaborates cross-functionally to uphold quality standards, improve processes, and contribute to continuous improvement efforts. This position requires strong analytical skills, attention to detail, and the ability to work independently in a dynamic manufacturing environment.
Job Duties & Responsibilities :
Assures consistent quality and oversees inspection, physical test methods and procedures. Enforces good manufacturing practices and systems by verifying processes and reviewing documentation. Achieves quality by contributing information and preparing and completing action plans; identifying and resolving problems; determining system improvements; implementing change, enforcing policies and procedures. Accomplishes quality objectives; analyzes variances and initiates corrective actions. Supports quality processes by documenting evidence, identifying critical control points and preventative measures by monitoring procedures and verification of procedures. Assists in writing and updating quality procedures. Maintains and improves product quality by surveillance audits, company policies, systems, procedures, and compliance. Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Responsible for conducting testing procedures on equipment during manufacturing processes to ensure that products comply with quality standards. Focuses on various procedures throughout the manufacturing process; Inspection of finished goods to find defects, check weights, etc. Oversees the rework process by inspection and physical test methods and procedures. Pulling incoming raw and finished samples for testing, inspect and verify incoming and outgoing product and paperwork to ensure that products comply with quality standards. Oversees and updates in-process product inspection standards. Maintains product quality by enforcing quality policies and procedures. Accurately update quality logs; Lab submission, skip lot testing, MRB and expired products. Sample, perform and document thorough examinations of all materials and finished products. Conduct and report internal audits and evaluations. Implement and improve quality control operating procedures. Supports the management of outside lab testing, material review, and release procedures. Administers a timely turnaround on OOS, NCR, or CAPA activities especially relating to incoming raw materials and finished product prior to release. Performs in-process or incoming material testing in-house as needed on equipment housed within the sampling laboratory. Acts as an indirect lead of other quality technicians to coach and monitor performance as needed to report up to quality management. Can act in place of quality tech I position to cross cover areas when department might be shorthanded. Can act as a provisional backup for Quality Supervisor if Director or Assistant Manager assign. Other projects as assigned. Adheres to cGMP within production areas of facility, monitors and enforces other team members adherence to requirements. Possesses a higher level of understanding of cGMP requirements and has the ability to coach and train fellow employees on appropriate compliance with standards. Responsible for monitoring and reporting on consumable items and inventory, equipment calibration and performance, and other items as needed to maintain an effective sampling/testing lab and process. As a higher-level employee within the quality unit, this position facilitates interdepartmental cooperation for the purposes of effective production and continuously improving a companywide culture committed to high standards of quality in all aspects of manufacturing. Maintain a clean and safe work environment. Qualifications:
High School Diploma or GED Preferred. Equivalent experience will be considered on a case-by-case basis. Previous work experience in quality control or other related fields Strong attention to detail Strong analytical and critical thinking skills Excellent written and verbal communication skills Proficient in Microsoft Office A proficiency in reading and writing English to meet FDA record keeping requirements. Competency in adding, subtracting, multiplying, dividing, calculating percentages, and determining the simple mathematical formulas to be used. Frequent walking, standing, bending, and reaching throughout the shift. Ability to lift up to 20 pounds. Compliance with GMP environment and PPE requirements.
4/10 schedule 4 PM - 2:30 AM Monday - Thursday
PM Shift 4 PM - 2:30 AM
Job Summary:
The Quality Technician II plays a key role in ensuring product integrity and regulatory compliance throughout the manufacturing process. This position is responsible for performing in-depth inspections, testing, and documentation of raw materials, in-process components, and finished goods. The role supports quality initiatives by enforcing GMP standards, executing internal audits, resolving non-conformances, and implementing corrective actions. Acting as a mentor and indirect lead to junior quality staff, the Quality Technician II collaborates cross-functionally to uphold quality standards, improve processes, and contribute to continuous improvement efforts. This position requires strong analytical skills, attention to detail, and the ability to work independently in a dynamic manufacturing environment.
Job Duties & Responsibilities :
Assures consistent quality and oversees inspection, physical test methods and procedures. Enforces good manufacturing practices and systems by verifying processes and reviewing documentation. Achieves quality by contributing information and preparing and completing action plans; identifying and resolving problems; determining system improvements; implementing change, enforcing policies and procedures. Accomplishes quality objectives; analyzes variances and initiates corrective actions. Supports quality processes by documenting evidence, identifying critical control points and preventative measures by monitoring procedures and verification of procedures. Assists in writing and updating quality procedures. Maintains and improves product quality by surveillance audits, company policies, systems, procedures, and compliance. Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Responsible for conducting testing procedures on equipment during manufacturing processes to ensure that products comply with quality standards. Focuses on various procedures throughout the manufacturing process; Inspection of finished goods to find defects, check weights, etc. Oversees the rework process by inspection and physical test methods and procedures. Pulling incoming raw and finished samples for testing, inspect and verify incoming and outgoing product and paperwork to ensure that products comply with quality standards. Oversees and updates in-process product inspection standards. Maintains product quality by enforcing quality policies and procedures. Accurately update quality logs; Lab submission, skip lot testing, MRB and expired products. Sample, perform and document thorough examinations of all materials and finished products. Conduct and report internal audits and evaluations. Implement and improve quality control operating procedures. Supports the management of outside lab testing, material review, and release procedures. Administers a timely turnaround on OOS, NCR, or CAPA activities especially relating to incoming raw materials and finished product prior to release. Performs in-process or incoming material testing in-house as needed on equipment housed within the sampling laboratory. Acts as an indirect lead of other quality technicians to coach and monitor performance as needed to report up to quality management. Can act in place of quality tech I position to cross cover areas when department might be shorthanded. Can act as a provisional backup for Quality Supervisor if Director or Assistant Manager assign. Other projects as assigned. Adheres to cGMP within production areas of facility, monitors and enforces other team members adherence to requirements. Possesses a higher level of understanding of cGMP requirements and has the ability to coach and train fellow employees on appropriate compliance with standards. Responsible for monitoring and reporting on consumable items and inventory, equipment calibration and performance, and other items as needed to maintain an effective sampling/testing lab and process. As a higher-level employee within the quality unit, this position facilitates interdepartmental cooperation for the purposes of effective production and continuously improving a companywide culture committed to high standards of quality in all aspects of manufacturing. Maintain a clean and safe work environment. Qualifications:
High School Diploma or GED Preferred. Equivalent experience will be considered on a case-by-case basis. Previous work experience in quality control or other related fields Strong attention to detail Strong analytical and critical thinking skills Excellent written and verbal communication skills Proficient in Microsoft Office A proficiency in reading and writing English to meet FDA record keeping requirements. Competency in adding, subtracting, multiplying, dividing, calculating percentages, and determining the simple mathematical formulas to be used. Frequent walking, standing, bending, and reaching throughout the shift. Ability to lift up to 20 pounds. Compliance with GMP environment and PPE requirements.
4/10 schedule 4 PM - 2:30 AM Monday - Thursday