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Pharma Injectable Jobs (NOW HIRING)

Therapeutic Sales Specialist

Atlanta, GA · Remote

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

Therapeutic Sales Specialist

Queens, NY · On-site

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

Therapeutic Sales Specialist

Columbia, SC · On-site

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

Therapeutic Sales Specialist

Atlanta, GA · On-site

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

Therapeutic Sales Specialist

Queens, NY · Remote

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

Therapeutic Sales Specialist

Syracuse, NY · On-site

$130K - $170K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

$125K - $165K/yr

As a Therapeutic Sales Specialist, you'll represent LEO Pharma Inc. within an assigned territory ... Experience selling sub-cutaneous self-injectable (or office administered IC) biologics preferred

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Showing results 1-20

Pharma Injectable information

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$14

$45

$75

How much do pharma injectable jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for pharma injectable in the United States is $45.24, according to ZipRecruiter salary data. Most workers in this role earn between $31.01 and $55.53 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities for a Pharma Injectable?

In a Pharma Injectable position, your day-to-day tasks usually include overseeing the aseptic preparation and filling of injectable products, conducting in-process quality checks, and ensuring compliance with safety and regulatory standards. You may also be involved in equipment calibration, documentation of batch records, and coordinating with quality assurance and engineering teams to resolve production issues. Collaboration is often needed across departments to maintain product integrity and streamline production flow. This role requires meticulous attention to cleanliness and detail to prevent contamination and ensure consistent quality. Working in this environment offers valuable experience in sterile manufacturing and deepens your expertise in the rapidly growing injectables segment of the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a Pharma Injectable?

To thrive in a Pharma Injectable role, you need a solid understanding of pharmaceutical manufacturing processes, sterile techniques, and regulatory compliance, typically supported by a degree in pharmacy, chemistry, or related fields. Familiarity with Good Manufacturing Practices (GMP), sterile filling equipment, and quality control systems is essential. Strong attention to detail, effective teamwork, and clear communication are vital soft skills for ensuring product quality and safety. These qualifications and skills are crucial for maintaining high standards and regulatory compliance in the production of injectable pharmaceuticals.

What is a Pharma Injectable?

A Pharma Injectable job involves the manufacturing, quality control, regulatory compliance, and distribution of injectable pharmaceutical products. Professionals in this role work to ensure that injectable drugs meet strict safety and efficacy standards set by regulatory authorities. Responsibilities may include overseeing production processes, conducting quality assurance tests, and maintaining compliance with Good Manufacturing Practices (GMP). This role is critical in delivering sterile and effective medications used in hospitals, clinics, and other healthcare settings.

More about Pharma Injectable jobs
Infographic showing various Pharma Injectable job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $94,103 per year, or $45.2 per hour.

Lead Quality Assurance Specialist 2nd Shift

QuVa Pharma

Sugar Land, TX • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago


QuVa Pharma rating

7.7

Company rating: 7.7 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

55th of 86 rated pharmaceutical


Job description

Our Lead Quality Assurance Specialist 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 oversight and performance of functional areas, and training in regard to processes and documentation as they pertain to quality standards and governmental regulations. 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 full-time role for our second shift, working Monday through Friday from 2:00 PM to 10:30 PM. This is a set, consistent schedule based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.
What Lead Quality Assurance Specialist Does Each Day:
  • Ensures company compliance to QuVa Pharma's Standard Operating Procedures (SOPs) and Quality Management System (QMS)
  • Follows all regulatory guidelines, cGMP guidelines, and aseptic techniques as required by the job function
  • Works in accordance with area Supervision to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMPs) including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review, batch disposition, and product distribution as applicable
  • Supports department supervision in oversight and prioritization of day-to-day responsibilities.
  • Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMP
  • Demonstrates a high level of discretion in the timely identification, and resolution of events potentially impacting the Quality of products and processes
  • Provides an established technical expertise for current processes and oversees training of department personnel on new processes
  • Maintenance of retained sample storage
  • Reviews routine manufacturing, environmental monitoring and quality control data for in-process and finished products
  • Evaluation of batches / product for compliance with defined specifications
  • Sampling, inspection, and control of commercial product labels
  • Review and approval of shipping documentation for commercial products

Our Most Successful Lead Quality Assurance Specialists:
  • Work to create an environment of open communication, participation and information-sharing within and between teams within Quality Assurance and throughout facility
  • Are detail-oriented with strong verbal and written communications skills
  • Support the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards
  • Act decisively with purposeful pursuit of goals or objectives, and thinks strategically in terms of solutions
  • Drive achievement, expresses energy, shows accountability, ability to multi-task and work in a fast-paced, quality-rich environment
  • Motivate others, share knowledge, build high performing teams, show respect towards others, and give constructive feedback

Minimum Requirements for this Role:
  • A High School diploma or equivalent
  • Able to successfully complete a drug and background check
  • Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
  • 18+ years of age
  • 20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision test
  • Demonstrated performance with direct supervision of a team is required
  • At least 2 years' experience in Quality Assurance, Sterile Compounding and/or GMP production facility preferred
  • Strong Microsoft Word and Excel skills
  • 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:
  • Bachelor's Degree in life science or related field preferred but not required
  • At least 1 year experience at Quva Pharma preferred
  • At least 2 years' experience with FDA-regulated operations (cGMP processes) preferred

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

About Quva:
Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.
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."
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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