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Master Control Operator Jobs in Massachusetts (NOW HIRING)

Nova Biomedical

Senior Quality Engineer

Billerica, MA

$94K - $127K/yr

Minitab.Previous experience working with Master Control and/or Power BI a plus. * Auditing ... Proficiency in operating tools, machinery, or technical equipment. * Use of appropriate personal ...

Nova Biomedical

Senior Quality Engineer

Billerica, MA

$94K - $127K/yr

Minitab.Previous experience working with Master Control and/or Power BI a plus. * Auditing ... Proficiency in operating tools, machinery, or technical equipment. * Use of appropriate personal ...

Nova Biomedical

Senior Quality Engineer

Norwood, MA · On-site

$100K - $135K/yr

Prepare and review Engineering Change Orders (ECO) and Manufacturing Variances (MV) for operating ... Minitab * Previous experience working with Master Control and/or Power BI a plus * Auditing ...

Nova Biomedical

Senior Quality Engineer

Norwood, MA

$100K - $135K/yr

Prepare and review Engineering Change Orders (ECO) and Manufacturing Variances (MV) for operating ... Minitab * Previous experience working with Master Control and/or Power BI a plus * Auditing ...

Amrize

Quality Control Technician

Littleton, MA · On-site

$19.25 - $24.50/hr

Ensures Company vehicle is operated and maintained according to best practice and specified ... Master's degree Field of Study Preferred: Engineering or Science Required Work Experience: 5 - 7 ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

... operated to support reliable testing and maintain data integrity. * Ensure laboratory data ... * BS or master's degree in chemistry, biology, or other pharmaceutical science related field.

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All JobsMaster Control Operator JobsMaster Control Operator Jobs in Massachusetts

Master Control Operator information

See Massachusetts salary details

$15

$23

$33

How much do master control operator jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for master control operator in Massachusetts is $23.59, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $26.25 per hour, depending on experience, location, and employer.

What is a master control operator?

A Master Control Operator is a broadcast professional responsible for ensuring that television or radio programming is aired correctly and on schedule. They monitor the transmission of content, troubleshoot technical issues, and manage the switching of live and pre-recorded segments. This role is crucial in maintaining broadcast quality, adhering to schedules, and complying with regulatory requirements. Master Control Operators also log broadcasts and may perform basic equipment maintenance. Their work is essential for the smooth operation of television and radio stations.

What is a master control operator?

A master control operator monitors and records television broadcasts to ensure quality and compliance with government regulations. As a master control operator, your duties include observing and recording satellite, cable, or live on-air programs, and using technology to record, dub, or make other adjustments to the broadcasts. To pursue a career as a master control operator, you need at least a high school diploma or GED certificate and relevant work experience. Some employers prefer candidates with a college degree in communications, journalism, or a related field and technical skills training. Additional qualifications include attention to detail, technical knowledge to operate broadcast equipment and troubleshoot malfunctions, and the ability to archive and organize large amounts of media.

What are the key skills and qualifications needed to thrive as a master control operator, and why are they important?

To thrive as a Master Control Operator, you need a solid understanding of broadcast operations, signal flow, and video/audio quality control, often supported by a degree in communications or related experience in broadcasting. Familiarity with automation systems, broadcast consoles, and scheduling software is typically required, along with relevant certifications like SBE (Society of Broadcast Engineers) credentials. Attention to detail, problem-solving skills, and the ability to work calmly under pressure are crucial soft skills for this role. These competencies ensure seamless transmission, regulatory compliance, and quick resolution of technical issues in live broadcast environments.

What are some common challenges faced by master control operators and how can they be addressed?

Master Control Operators often encounter challenges such as managing multiple live feeds, troubleshooting technical issues under tight deadlines, and maintaining broadcast quality during unexpected disruptions. Staying organized, keeping calm under pressure, and having a strong understanding of broadcast equipment are crucial for success. Effective communication with engineering teams and other departments also helps quickly resolve problems and minimize on-air interruptions.

What is the difference between Master Control Operator vs Broadcast Technician?

AspectMaster Control OperatorBroadcast Technician
CredentialsHigh school diploma; certifications varyHigh school diploma; technical certifications often preferred
Work EnvironmentTV/radio stations, cable networks, broadcasting facilitiesBroadcast stations, production companies, technical support
Job FocusMonitoring and controlling live broadcasts, ensuring signal qualityInstalling, maintaining, repairing broadcast equipment

While both roles support broadcasting operations, the Master Control Operator primarily manages live broadcasts and signal quality, whereas the Broadcast Technician focuses on technical maintenance and equipment repair. Understanding these differences helps clarify career paths and job expectations in the broadcasting industry.

Is being a master control operator hard?

Master control operators are responsible for monitoring and managing broadcast signals, which requires attention to detail, technical skills, and the ability to handle live situations. The job can be demanding due to irregular hours, the need for quick problem-solving, and familiarity with broadcast equipment and automation systems.
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Master Control Operator jobs near you
Infographic showing various Master Control Operator job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 2% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $49,060 per year, or $23.6 per hour.

Packaging Documentation Specialist - MDI

Cipla

Fall River, MA • On-site

$66K - $86K/yr

Full-time

Posted 18 days ago

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.
Job Title: Packaging Documentation Specialist - MDI
FLSA Classification: Professional, Exempt
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To: Packaging Manager
Salary Range: $66,300 - $86,000
Job Overview
Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist.
The Manufacturing Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well as SOP's. In this role the Documentation Specialist adheres to the company's document and SOP's procedures while ensuring their accuracy, quality, and integrity. This position reports to the Site Lead/Operation Manager and partners with cross functional team members to ensure compliance and operational success through user focused documentation at InvaGen Pharmaceuticals, Inc, Fall River, MA.
The job duties for this position include but are not limited to the following:
  • Works with Manufacturing/Packaging to deliver timely batch record review across all shifts.
  • Reviews and approval of master batch records.
  • Develops appropriate disposition metrics, works with manufacturing/packaging personnel to achieve said targets. Generates and reports on metrics on agreed frequency
  • Creates training materials for subject matter input.
  • Track and manage periodic review of approved procedures.
  • Develop strategies and documents for cleaning and process validation of equipment and products in compliance with site SOPs and regulatory guidance.
  • Provides data to support management evaluation of performance trends.
  • Owns quality records (change control, CAPA's, deviations) and delivers to established timelines.
  • Autonomously leads and manages projects to implement continuous improvement opportunities.
  • Lead and/or support root cause investigations related to performance trends and formal deviations.
  • Develop, implement and assess solutions for complex problems.
  • Anticipates risk and builds contingencies to help mitigate impact.
  • Reviews document for accuracy and completeness.
  • Defends the validation programs and strategies to customers and regulatory auditors.
  • Performs weekly quality reviews of Master Control database by assuring new documents have been entered using appropriate protocols.
  • Follows strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring the environment.
  • Performs other duties as assigned.

Education and Experience
  • Associate degree with 1-3 years knowledge and experience of GMP documentation required.
  • Bachelor's degree in science, biochemistry, pharmaceutical engineering, Pharmaceutical Sciences, or related discipline from an accredited college/university.
  • Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.
  • Minimum one (1) year documentation experience and three (3) years related pharmaceutical or biotech industry experience. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.

Technical Knowledge and Computer Systems Skills
  • Excellent communication skills, drive, and sense of urgency
  • Excellent computer skills, specifically Microsoft Office Suite.
  • Solid organizational and time management skills are required to prioritize activities in a manner consistent with departmental and site wide objectives.
  • Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring the environment.
  • Must have ability to work as self-starter and handle multiple priorities in a dynamic cross-functional team-based environment.
  • Knowledge of pharmaceutical manufacturing and related documents.
  • Knowledge and experience writing, revising and creating cGMP records and SOP's.
  • Knowledge of GDP.
  • Creation and maintenance of batch record and cGMP documentation templates.
  • Closure of any compliance related CAPA's.
  • Hands-on experience facilitating problem solving and root cause investigations in a pharmaceutical environment - Develops, implements, and assesses solutions for complex problems.
  • Ability to work effectively both independently and as part of a team.
  • Capable of handling and participating in compliance and regulatory audits at the local and federal levels.
  • Experience using SAP business system and applications is a plus.
  • Experience in Inhalation products (MDI) is a plus.
  • Knowledge and handling of deviation, CAPA, change control, FMECA, OOS, OOT, training and OOAC.
  • Knowledge and handling of SAP system, master control and TrackWise system.
  • Knowledge of preparation of BMR and eBMR.
  • Knowledge of preparation of SOP and eLog books.
  • During audit part of team.
  • Planning of batches as per production plan.
  • Knowledge of audits and compliance.

Professional and Behavioral Competencies
  • Proficiently speak English as a first or second language
  • Ability to understand and analyze complex data sets.
  • Knowledge of statistical packages is a plus.
  • Knowledge of good manufacturing practices and good documentation practices preferred.
  • Ability to read, write and communicate effectively.
  • Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.
  • Position requires flexibility to quickly adapt to changing work environment and schedules
  • Excellent organizational skills with the ability to focus on details.
  • Basic computer skills (Word and Excel) - Intermediate
  • Good basic math knowledge and excellent attention to details.

Work Schedule and Other Position Information
  • Must be willing to work in a pharmaceutical manufacturing setting.
  • Must be willing to work some weekends based on business needs as required by management.
  • Relocation negotiable.
  • No remote work available.

GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.
Cipla, Inc is an equal opportunity and affirmative action employer committed to building an inclusive and diverse workforce.

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