Lead Production Technician - Formulator 2Nd Shift

Our Lead Production Technician

• Formulator plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include daily coordination and working schedules for the formulations teams that are assigned to work in a specific area. Oversees planning, scheduling and daily execution for the formulation/manufacture of bulk and non-sterile products in the controlled and classified areas. Will support training of new formulators in daily manufacturing activities for non-sterile and sterile bulk/CSP operations such as; chemical weighing, sterile filter integrity testing, aseptic cleaning and disinfection of cleanroom, active ingredient inventory controls. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

What the Lead Production Technician

• Formulator Does Each Day:

• Oversee activities, including scheduling dispensing, formulating, cleaning, compounding and sterile filtration activities

• Oversee and supports the dispensing of chemicals and raw materials that will be used to manufacture bulk intermediate products

• Oversee and supports preparation of bulk intermediate solutions that will be used in compounded sterile products

• Complete necessary documents for accountability and traceability of product following Good Documentation Practices (GDPs); Comply with cGMPs, and company ISO standards

• Comply with 503B guidelines; cGMPs, and company standards

• Maintain Daily/ Bi-Weekly/Monthly cleaning of processing room and equipment and fill out appropriate preventative maintenance forms and checklists in accordance with SOP's

• Immediate notification of production management of deviations to established processes or procedures

• Pass & maintain Gown qualification

• Pass & maintain Bulk Bag Media Fill Qualification

• Perform training of on-the-job skills

Our Most Successful Lead Production Technician

• Formulator:

• Work with the area supervisor to manage daily activities of the formulation technicians to meet production schedule

• Maintain Daily/ Bi-Weekly/Monthly cleaning of processing room and equipment

• Timely address and escalate process nonconformities in batch formulation as appropriate

• Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization

• Maintain documentation, including batch documentation in accordance with Good Documentation Practices; has strong math skills

• Effectively and productively engages with others and establishes trust, credibility, and confidence with others

Minimum Requirements for this Role:

• High school Diploma or GED from recognized institution or organization

• Demonstrated performance with direct supervision of a team

• At least 1-year pharmaceutical manufacturing experience

• Strong Math skills

• Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas

Any of the Following Will Give You an Edge:

• College Degree with an emphasis in Chemistry, Biochemistry or equivalent

Benefits of Working at QuVa:

• Set, full-time, consistent work schedule

• Comprehensive health and wellness benefits including medical, dental and vision

• 401k retirement program with company match

• 17 paid days off plus 8 paid holidays per year

• Occasional weekend and overtime opportunities with advance notice

• National, industry-leading high growth company with future career advancement opportunities

About QuVa:

QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.

As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.

QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is "at will."