Alcon

Production Support Supervisor, Nights

Alcon$85K — $158K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 3 years in pharmaceutical manufacturing or 5 years without degree.
  • Strong knowledge of cGMP regulations and FDA guidelines.
  • Ability to work in cleanroom environments and wear full PPE for extended durations.
  • Flexibility to work rotating night shifts and extended hours.
  • Capability to lift or carry up to 35 pounds.

Responsibilities

  • Execute manufacturing support for radioligand drug products, maintaining high standards.
  • Ensure compliance with Standard Operating Procedures and batch records during production.
  • Prepare and verify materials while maintaining identity according to procedures.
  • Conduct routine and dynamic environmental monitoring for compliant manufacturing environments.
  • Complete and review essential production documentation including batch records and training logs.
  • Participate in qualification/validation activities and support product packaging.
  • Ensure technician training completion, promoting team capability and compliance.

Benefits

  • Comprehensive health, life and disability insurance.
  • 401(k) with company contribution and match.
  • Generous time off package including vacation, personal days, and holidays.
  • Eligibility for annual equity awards and performance-based cash incentives.
Full Job Description

Band

Level 3

Job Description Summary

Location: Carlsbad, California

Relocation Support: This role is based in Carlsbad, California. Novartis is unable to offer relocation support: please only apply if accessible.

You will help deliver life-changing radioligand therapies to patients while leading critical overnight manufacturing operations. As a Production Support Supervisor, you will combine hands-on expertise with frontline leadership—overseeing the setup and preparation of instruments and equipment, and ensuring every batch is produced safely, efficiently, and to the highest quality standards.

NOTE: Two positions are available working 12-hour rotating shifts. One position will work Sunday – Wednesday and the second will work Wednesday – Saturday. Shift hours are expected to be 6 pm – 7 am. Periodic mandatory overtime may be necessary to ensure process continuity and completion.


 

Job Description

Key Responsibilities

  • Execute all activities supporting the manufacturing of radioligand drug products, including operating and maintaining Grade C isolators, manually cleaning the cell, and performing sterilization of the isolators
  • Ensure adherence to Standard Operating Procedures and batch records throughout all production activities
  • Prepare and verify materials, maintaining material identity in accordance with defined procedures
  • Conduct routine and dynamic environmental monitoring to support compliant manufacturing conditions
  • Complete and review production documentation, including batch records, shipping documents, and training records
  • Participate in assigned qualification/validation activities and support packaging of finished product, as necessary.
  • Ensure technician training completion and support ongoing development to build a capable and compliant team
  • Promote a culture of quality, safety, and compliance, encouraging accountability and continuous improvement across the team

Essential Requirements

  • Bachelor’s degree with 3 years of pharmaceutical manufacturing experience or 5 years of pharmaceutical manufacturing experience required without degree. 
  • Strong knowledge of cGMP regulations and FDA guidance including solid understanding of manufacturing operations, validation processes, and production documentation requirements
  • Ability to work in cleanroom environments, wearing full personal protective equipment for extended periods
  • Flexibility to work night shifts and support extended hours to maintain continuous manufacturing operations
  • Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.
  • Makeup, jewelry, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas.
  • Ability to lift or carry up to 35 pounds.

Desirable Requirements

  • Training in radiochemistry or radio pharmacy
  • Prior experience with low bioburden manufacturing

The salary for this position is expected to range between $85,400 and $158,600 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.


 

Salary Range

$85,400.00 - $158,600.00


 

Skills Desired

General Hse Knowledge  , gmp knowledge

About Alcon

Alcon is a global medical company specializing in eye care products and services. The company's products include surgical equipment, contact lenses, and eye drops. Alcon was founded in 1945 and is headquartered in Baar, Switzerland. The company operates in over 70 countries and has over 20,000 employees. In 2019, Alcon became an independent publicly traded company after being spun off from Novartis.
Learn more about Alcon
Size
24,389 employees
Market Cap
$33.3 billion
Industry
Founded
1945
NASDAQ

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