Manager, Manufacturing Operations 3Rd Shift

Our Manager, Manufacturing Operations 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 managing the manufacturing of sterile pharmaceuticals within the facility. The primary function is to oversee all operations, and personnel, of Inspection, Labeling and Packaging Operations where multiple requirements and challenges will exist requiring a good knowledge base and ability to apply operational, quality, and regulatory skill sets. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What Manager, Manufacturing Operations Does Each Day:

• Manages staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements

• Manages operations to assure all products are visually inspected, labeled and packed into their finished containers as per applicable standard operating procedure

• Prepares and submits weekly/monthly reports, prepares metrics and trends data to identify and prioritize continuous improvement opportunities

• Establishes & maintains cooperative cross-functional relationships with peers in Quality, and other manufacturing operations colleagues to meet plant objectives

• Leads in development & maintenance of a safe manufacturing environment. Participates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminate hazardous conditions

• Counsels, trains, & develops front line leaders for efficient performance and assists in their career development; creates an atmosphere of team effort & open communication

• Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure

Our Most Successful Manager, Manufacturing Operations:

• Has Strong technical writing and verbal/written communication skills, including presentation skills

• Has excellent interpersonal skills demonstrating the ability to interact with people holding positions in many different departments

• Has successful time management skills to coordinate successful accomplishment of an approved action plan with timelines and milestone tasks

• Recognizes priorities and acts, makes productive use of time

• Develops action plans to meet a specific objective including identification and methods of tasks, milestones, resources requirements and metrics

Minimum Requirements for this Role:

• Bachelor's Degree in Life Science or another related field

• 3 years of supervisory or management experience

• Hands-on direct shop floor involvement: Troubleshooting

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

Any of the Following Will Give You an Edge:

• 3 years prior experience in cGMP / FDA regulated industry

• Understanding of process flows, gap assessments and analysis of data to drive improvement

• Proficiency with computerized tracking tools

• Comprehensive knowledge of adult learning techniques

Benefits of Working at QuVa:

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

• 401k retirement program with company match

• 22 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."