Weekend Operations Supervisor

Serán BioScience seeks a uniquely qualified candidate to fill our Weekend Operations Supervisor role. Helping to complete a fully supervised manufacturing team that operates seven days a week, this Supervisor will be scheduled primarily during the days of Friday, Saturday and Sunday. Additional coverage or collaboration to support the department may be requested.

As a supervisor, you will play an integral role in maintaining specialized equipment for the manufacturing of tablets, capsules and spray drying dispersion for the use of early phase clinical FDA trials. Enforcing strict standard operating procedures (SOP) and following good manufacturing practices (GMP) are required. Successful candidates will demonstrate strong leadership and motivational skills, attention to detail and focus within a fast-paced work environment with proven examples of self-discipline and proactive communication to ensure collective goals and production schedules are achieved. This role will oversee daily shift activities and perform manufacturing operations according to established procedures. This position is responsible for ensuring a high level of compliance with internal procedures and regulatory guidance.

Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a principled and positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.

Duties And Responsibilities

• Oversees daily shift activities and daily workflow of the production team
• Provides constructive and timely performance evaluations and feedback
• Follows strict standard operating procedures (SOPs)
• Writes and reviews standard operating procedures
• Weighs, measures, subdivides, and disposes of components
• Safely handles hazardous materials
• Participates in audits or inspections
• Inspects and maintains specialized manufacturing equipment
• Drafts, reviews, and approves quality records as technical approver
• Acts as subject matter expert for Spray Dry and/or Oral Solid Dosage manufacturing equipment
• Conducts and attends training activities
• Completes documentation, including logbooks and batch production and control records
• Works closely and communicates effectively with Operations, Quality and EMF departments   
• Adheres to schedule to meet time sensitive deadlines
• Performs other related duties as assigned.
  
  
  

Required Skills And Abilities

• Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
• Strong verbal and written communication skills
• Excellent organizational skills with attention to detail
• Excellent time management skills with a proven ability to meet deadlines
• Strong problem-solving skills
• Intermediate math skills
• Strong supervisory and leadership skills with proven ability to positively motivate teams
• Ability to prioritize tasks and to delegate them when appropriate
• Accepts feedback from a variety of sources and constructively manages conflict
• Ability to function well in a high-paced and at times stressful environments
• Proficient with Microsoft Office Suite or related software
• Proven mechanical aptitude
  
  
  

Education And Experience

• High school diploma or equivalent
• Proven experience in Spray Dry and/or Oral Solid Dosage Manufacturing
• Proficiencies in GMP processing and equipment
• Requires 3 year of GMP experience, five years preferred
  
  
  

Physical Requirements

• Prolonged periods of sitting or standing while monitoring equipment
• Must be able to lift up to 25 pounds regularly, and up to 55 pounds occasionally
• Ability to work weekend shift/12-hour shifts
• Must be able to wear a Tyvek suit with PAPR for extended periods of time
• Exposure to constant low-level equipment noise, and occasional high-level alarms
• Work near heat generating equipment
• Must be able to operate a forklift
• Move up and down ladders, kneel, squat, balance on one foot
• Move mop above head while cleaning room surfaces
  
  
  

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Compensation Will Be Based On Experience.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Benefits Summary:

Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.

The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701