Validation Technician

Unither Pharmaceuticals

City of Rochester (NY)

On-site

USD 27,813 - 34,440

Full time

14 days+
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

100% employer-paid medical premiums
401(k) contributions
Annual performance bonuses

Job summary

A leading pharmaceutical company in Rochester, NY, is seeking a team member to assist with validation efforts related to equipment and processes. The role requires a high school diploma or equivalent and experience in a FDA regulated environment. Ideal candidates will possess strong documentation skills and basic mechanical knowledge. This position offers competitive compensation and benefits including 100% employer-paid medical premiums.

Qualifications

  • Minimum 2 years of experience in a FDA regulated environment.
  • Above average written communication skills required.
  • Basic mechanical knowledge and aptitude necessary.

Responsibilities

  • Assists in execution of validation protocols for manufacturing processes.
  • Maintains department documentation for regulatory compliance.
  • Ensures good documentation practices are followed.

Skills

Basic math skills
Familiarity with MS Word and Excel
Basic mechanical knowledge
Ability to learn equipment operation
Good communication skills

Education

HS Diploma/GED
AAS
BS

Tools

Basic hand tools

Job description

Who we are?

We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible.

With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees.

Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow‑Fill‑Seal, Liquid Stick‑Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 300 employees.

Your role

Reporting to the Director of Quality,

JOB SUMMARY:

Assists validation efforts in many ways including the following: executes/supports equipment qualifications, cleaning validations and recertifications, chamber (i.e., freezers, refrigerators, incubators) recertifications, and process validations, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining the Validation Document Library, maintains test equipment and department documentation.

Essential Functions / Responsibilities
  • Assists in the execution of validation protocols (qualification, process validations, and recertifications) for facilities, chambers, manufacturing equipment, manufacturing processes, cleaning, and critical utilities.
  • Performs proper and timely post cleaning sampling from manufacturing equipment. Confirms there is an appropriate amount of required sampling materials and supplies available. Orders are to be placed as needed to ensure supplies are maintained. Responsible for organization of supplies and materials, FIFO is consistently followed.
  • Maintains department documentation in an orderly library so that information can be provided to regulatory bodies in a timely manner. Participates in audits (i.e., customer and regulatory) and retrieves validation documentation as requested.
  • Ensures good documentation practices are followed during protocol executions, verifications, validation plans and summary reports generated during validation/qualification activities are maintained according to procedure.
  • Becomes proficient using temperature/humidity loggers along with the associated DT Pro software. Responsibilities will include, programming, reading, generating reports, as well as conducting routine maintenance per department procedure.
  • Reviews documentation executed during validation activities and ensures completeness is performed contemporaneously. All applicable documentation is scanned and transferred to the activity’s applicable project folder and all completed hardcopies are filed accurately within the site’s documentation room.
  • Ensures all department testing equipment is maintained in a current calibrated state. Communicates and works with outside vendors to schedule, ship, track, and receive testing equipment to be sent for calibration. Confirms a current calibration certificate is received with each piece of testing equipment. Inventory and calibration status is maintained within Blue Mountain Regulatory Asset Manager (BMRAM).
Your Profile
Education & Experience
  • HS Diploma/GED with minimum 2 years of experience in a FDA regulated environment, GMP production setting preferred.
  • AAS with 1 year experience in a FDA regulated environment, GMP production setting preferred.
  • BS with 0 experience.
  • Above average written communication skills & writing abilities.
  • Basic mechanical knowledge and aptitude.
  • Ability to learn the operation and function of multiple pieces of equipment.
  • Use of basic hand tools such as wrenches, screwdrivers, measuring devices.
  • Knowledge of computer applications and current software is desirable.
  • Knowledge of manufacturing processes and demonstrated leadership capabilities are preferred.
  • General understanding of material handling machinery is advantageous.
Knowledge, Skills & Abilities
  • Demonstrated basic math skills in multiplication, division, percentage calculation, significant figures, conversion from metric to standard measures (or inverse), and weight to volume measures (or inverse). This would include basic algebra and geometry.
  • Familiarity using MS Word and Excel. An understanding of production activities and/or mechanical aptitude.
  • Knowledge of production equipment operations.
  • Knowledge of instrumentation, control systems, and production equipment.
  • Must be able to recognize situations where there is a potential impact on product quality, safety, identity and purity; seeking guidance where necessary to implement solutions to issues that are identified.
  • Ability and willingness to support transactional and administrative functions within the department.
  • Requires good teamwork, excellent communication, interpersonal and organization skills.
SCOPE OF DECISION-MAKING

Decisions require some judgment and critical thinking ability. Perform repetitive or routine duties working from detailed instructions and under standard procedures. Requires making minor decisions.

Compensation Range

20.19 - 25.00 USD

The referenced compensation range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.

A Smarter Total Compensation Package
  • 100% employer‑paid medical premiums (a $2,000–$6,000+ annual value)
  • 401(k) contributions: 6% match plus an additional 4% company‑funded contribution
  • HSA contributions with wellness incentives
  • Annual performance bonuses and merit increase eligibility
  • And more—because we invest in your health, your future, and your peace of mind.

It’s a package designed to reward impact—not just hours worked.

More Than Just a Paycheck

At Unither, we don’t just offer competitive hourly wages—we also pay 100% of your medical premiums. That means no paycheck deductions for your healthcare, which can be worth an extra $1 to $3.50 an hour in your pocket compared to jobs where you pay part of the premium.

Learn more about us

We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees. Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives.

We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential. We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility.

Join us and make a difference!

Equal Employment Opportunity

Unither is an Equal Opportunity Employer. We are committed to providing reasonable accommodations for qualified individuals with disabilities and to ensuring equal employment opportunity for all applicants.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Validation Specialist
Validation Specialist

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 60,000 - 75,000
100% employer-paid medical premiums
401(k) contributions
Paid time off
Packaging Supervisor- C Shift
Packaging Supervisor- C Shift

Unither Pharma • City of Rochester (NY), Northern (KY)

On-site
USD 82,000 - 92,000
Medical premiums paid
401(k) match
HSA contributions
+1
Manufacturing Equipment Operator - Sterile C Shift
Manufacturing Equipment Operator - Sterile C Shift

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 26,174 - 28,929
Employer-paid medical premiums
401(k) with match
HSA contributions
+2
Packaging Supervisor- B Shift
Packaging Supervisor- B Shift

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 82,000 - 92,000
Employer-paid medical premiums
401(k) with match
HSA contributions
+1
Quality Systems Specialist II
Quality Systems Specialist II

Unither Pharma • City of Rochester (NY), Northern (KY)

On-site
USD 80,000 - 90,000
Employer-paid medical premiums
Retirement savings with 401(k) match
HSA contributions
+1
Quality Systems Specialist II
Quality Systems Specialist II

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 80,000 - 90,000
Medical premiums paid
401(k) match
Annual bonuses
+1
Mechanical/Electrical Engineer
Mechanical/Electrical Engineer

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 85,000 - 95,000
100% employer-paid medical premiums
401(k) contributions with match
Annual performance bonuses
+1
Manufacturing Equipment Operator- C Shift
Manufacturing Equipment Operator- C Shift

Unither Pharma • City of Rochester (NY)

On-site
USD 26,000 - 29,000
Employer-paid medical premiums
401(k) with company match
HSA contributions
Process Engineer
Process Engineer

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 80,000 - 95,000
Medical premiums fully paid
401(k) with match
HSA contributions
+1
Manufacturing Equipment Operator- C Shift
Manufacturing Equipment Operator- C Shift

Unither Pharmaceuticals • City of Rochester (NY)

On-site
USD 26,000 - 29,000
Employer-paid medical premiums
401(k) plan with company match
HSA contributions
+1